A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569068



Internal ID16009791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34579095hg38UCSC Ensembl
Innerchr15:34730758..34871296hg19UCSC Ensembl
Innerchr15:32518050..32658588hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38140539
hg19140539
hg18140539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4477n54
Supporting Variantsnssv840264, nssv840265
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569068
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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