A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861922



Internal ID16155878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81035642..81036290hg38UCSC Ensembl
Innerchr16:81069247..81069895hg19UCSC Ensembl
Innerchr16:79626748..79627396hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38649
hg19649
hg18649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573341
Supporting Variants
Samples
Known GenesATMIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861922
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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