A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569026



Internal ID16009749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435441..34476342hg38UCSC Ensembl
Innerchr15:34727642..34768543hg19UCSC Ensembl
Innerchr15:32514934..32555835hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3840902
hg1940902
hg1840902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4470n54
Supporting Variantsnssv840067, nssv840068
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569026
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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