A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569504



Internal ID16356913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54413704..54502842hg38UCSC Ensembl
Innerchr15:54705902..54795040hg19UCSC Ensembl
Innerchr15:52493194..52582332hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3889139
hg1989139
hg1889139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4541n54
Supporting Variantsnssv843293
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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