A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149666



Internal ID15530044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89207475..89319153hg38UCSC Ensembl
Innerchr16:89273883..89385561hg19UCSC Ensembl
Innerchr16:87801384..87913062hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38111679
hg19111679
hg18111679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573734
Supporting Variants
SamplesHGDP00885
Known GenesANKRD11, ZNF778
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149666
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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