A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149655



Internal ID15872974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53329773..53382710hg38UCSC Ensembl
Innerchr16:53363685..53416622hg19UCSC Ensembl
Innerchr16:51921186..51974123hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3852938
hg1952938
hg1852938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572618
Supporting Variants
SamplesHGDP00090
Known GenesLOC643802
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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