A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110453



Internal ID15963639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39377435..39385202hg38UCSC Ensembl
Innerchr8:39234954..39242721hg19UCSC Ensembl
Innerchr8:39354111..39361878hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg387768
hg197768
hg187768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610984
Supporting Variants
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110453
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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