A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685331



Internal ID18983612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20096917..20121792hg38UCSC Ensembl
Innerchr8:19954428..19979303hg19UCSC Ensembl
Innerchr8:19998708..20023583hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3824876
hg1924876
hg1824876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033931
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)nssv3685331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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