A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857858



Internal ID16151814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57332466..57333135hg38UCSC Ensembl
Innerchr16:57366378..57367047hg19UCSC Ensembl
Innerchr16:55923879..55924548hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38670
hg19670
hg18670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572719
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)nssv857858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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