A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573128



Internal ID16013851
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 StatusM
Merged Variants
Supporting Variantsnssv1149659
SamplesHGDP00677
Known GenesNUDT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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