A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692721



Internal ID18991002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135656274..135713488hg38UCSC Ensembl
Innerchr8:136668517..136725731hg19UCSC Ensembl
Innerchr8:136737699..136794913hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3857215
hg1957215
hg1857215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024283
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)nssv3692721
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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