A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569033



Internal ID16009756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435441..34508394hg38UCSC Ensembl
Innerchr15:34727642..34800595hg19UCSC Ensembl
Innerchr15:32514934..32587887hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3872954
hg1972954
hg1872954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4472n54
Supporting Variantsnssv840077, nssv840076
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569033
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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