A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569503



Internal ID16356912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54413704..54479682hg38UCSC Ensembl
Innerchr15:54705902..54771880hg19UCSC Ensembl
Innerchr15:52493194..52559172hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865979
hg1965979
hg1865979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843292
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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