A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610980



Internal ID16398389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375766..39385202hg38UCSC Ensembl
Innerchr8:39233285..39242721hg19UCSC Ensembl
Innerchr8:39352442..39361878hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg389437
hg199437
hg189437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12097n54
Supporting Variantsnssv1110448
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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