A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842495



Internal ID16136451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48060055..48111670hg38UCSC Ensembl
Innerchr15:48352252..48403867hg19UCSC Ensembl
Innerchr15:46139544..46191159hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3851616
hg1951616
hg1851616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569336
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)nssv842495
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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