A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568600



Internal ID16009323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26493638..26552355hg38UCSC Ensembl
Innerchr15:26738785..26797502hg19UCSC Ensembl
Innerchr15:24289878..24348595hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3858718
hg1958718
hg1858718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839150
Samples
Known GenesGABRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568600
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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