A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861696



Internal ID16155652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79819370..79905607hg38UCSC Ensembl
Innerchr16:79853267..79939504hg19UCSC Ensembl
Innerchr16:78410768..78497005hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3886238
hg1986238
hg1886238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573290
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)nssv861696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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