A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689722



Internal ID18988003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93274061..93302887hg38UCSC Ensembl
Innerchr8:94286289..94315115hg19UCSC Ensembl
Innerchr8:94355465..94384291hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3828827
hg1928827
hg1828827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033372
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)nssv3689722
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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