A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859121



Internal ID15806391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70690529..70697967hg38UCSC Ensembl
Innerchr16:70724432..70731870hg19UCSC Ensembl
Innerchr16:69281933..69289371hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387439
hg197439
hg187439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572948
Supporting Variants
Samples
Known GenesVAC14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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