A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859062



Internal ID16153018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63623386..63681930hg38UCSC Ensembl
Innerchr16:63657290..63715834hg19UCSC Ensembl
Innerchr16:62214791..62273335hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3858545
hg1958545
hg1858545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572892
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)nssv859062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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