A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838505



Internal ID16132461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23448259..23504661hg38UCSC Ensembl
Innerchr15:23693406..23749808hg19UCSC Ensembl
Innerchr15:21244499..21300901hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3856403
hg1956403
hg1856403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568340
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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