Product Details

Assay Reference Genome
Location

Chr.1:169512351 on build GRCh38
Cytoband
1q24.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
2153
Gene Symbol
F5
Gene Name
coagulation factor V
Gene Aliases
FVL, PCCF, RPRGL1, THPH2
Location
Chr.1:169511954-169586632 on build GRCh38
Assay Gene Location
Within Exon 25
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
F5 NM_000130.4 25 8782 NP_000121.2
XM_017000660.1 24 8791 XP_016856149.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv22143 Chr1:169090390 - 169652030 on Build GRCh38 Gain+Loss NME7 ATP1B1 F5 LOC101928596 SELP CCDC181 SLC19A2 BLZF1
nsv831871 Chr1:169351435 - 169517442 on Build GRCh38 Loss NME7 F5 CCDC181 SLC19A2 BLZF1

View Full Product Details