A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568754



Internal ID16009477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30635007..30802276hg38UCSC Ensembl
Innerchr15:30927210..31094479hg19UCSC Ensembl
Innerchr15:28714502..28881771hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38167270
hg19167270
hg18167270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4425n54
Supporting Variantsnssv839484
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568754
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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