A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639651



Internal ID18937932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8554326..8702116hg38UCSC Ensembl
Innerchr5:8554438..8702228hg19UCSC Ensembl
Innerchr5:8607438..8755228hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38147791
hg19147791
hg18147791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033498
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639651
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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