A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149659



Internal ID15528697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77660194..77727501hg38UCSC Ensembl
Innerchr16:77694091..77761398hg19UCSC Ensembl
Innerchr16:76251592..76318899hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3867308
hg1967308
hg1867308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573128
Supporting Variants
SamplesHGDP00677
Known GenesNUDT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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