A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149622



Internal ID15874042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20472407..20518912hg38UCSC Ensembl
Innerchr16:20483729..20530234hg19UCSC Ensembl
Innerchr16:20391230..20437735hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3846506
hg1946506
hg1846506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571619
Supporting Variants
SamplesHGDP00462
Known GenesACSM2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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