A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568962



Internal ID16009685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34413285..34414928hg38UCSC Ensembl
Innerchr15:34705486..34707129hg19UCSC Ensembl
Innerchr15:32492778..32494421hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381644
hg191644
hg181644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4464n54
Supporting Variantsnssv839848
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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