A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610949



Internal ID16051672
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1110016, nssv1110017
Samples
Known GenesADRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610949
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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