A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639025



Internal ID18590620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76787557..76833416hg38UCSC Ensembl
Innerchr5:76083382..76129241hg19UCSC Ensembl
Innerchr5:76119138..76164997hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3845860
hg1945860
hg1845860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031491
Supporting Variants
Samples
Known GenesF2RL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer