A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610948



Internal ID16051671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37963968..37967299hg38UCSC Ensembl
Innerchr8:37821486..37824817hg19UCSC Ensembl
Innerchr8:37940643..37943974hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383332
hg193332
hg183332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1110015
Samples
Known GenesADRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610948
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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