A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568912



Internal ID16009635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32609864..32619539hg38UCSC Ensembl
Innerchr15:32902065..32911740hg19UCSC Ensembl
Innerchr15:30689357..30699032hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg389676
hg199676
hg189676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4457n54
Supporting Variantsnssv839791
Samples
Known GenesARHGAP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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