A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569071



Internal ID16009794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34690183hg38UCSC Ensembl
Innerchr15:34730758..34982384hg19UCSC Ensembl
Innerchr15:32518050..32769676hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38251627
hg19251627
hg18251627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4468n54
Supporting Variantsnssv840272, nssv840273, nssv840270, nssv840268, nssv840274, nssv840269, nssv840271
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569071
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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