A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843298



Internal ID16137254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54584014..54612584hg38UCSC Ensembl
Innerchr15:54876212..54904782hg19UCSC Ensembl
Innerchr15:52663504..52692074hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828571
hg1928571
hg1828571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569508
Supporting Variants
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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