A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545963



Internal ID15986686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33254041..33354533hg38UCSC Ensembl
Innerchr1:33719642..33820134hg19UCSC Ensembl
Innerchr1:33492229..33592721hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38100493
hg19100493
hg18100493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712152
Samples
Known GenesA3GALT2, MIR3605, PHC2, ZNF362
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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