A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569131



Internal ID16009854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34579095..34728190hg38UCSC Ensembl
Innerchr15:34871296..35020391hg19UCSC Ensembl
Innerchr15:32658588..32807683hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38149096
hg19149096
hg18149096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840394
Samples
Known GenesGOLGA8B, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569131
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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