A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545962



Internal ID15986685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32982619..33129611hg38UCSC Ensembl
Innerchr1:33448220..33595212hg19UCSC Ensembl
Innerchr1:33220807..33367799hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38146993
hg19146993
hg18146993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712151
Samples
Known GenesADC, AK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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