A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110017



Internal ID15616517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37963968..37967856hg38UCSC Ensembl
Innerchr8:37821486..37825374hg19UCSC Ensembl
Innerchr8:37940643..37944531hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383889
hg193889
hg183889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610949
Supporting Variants
Samples
Known GenesADRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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