A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110055



Internal ID15963241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375062..39500465hg38UCSC Ensembl
Innerchr8:39232581..39357984hg19UCSC Ensembl
Innerchr8:39351738..39477141hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38125404
hg19125404
hg18125404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610967
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110055
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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