A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546659



Internal ID16334068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80071532..80165546hg38UCSC Ensembl
Innerchr1:80537217..80631231hg19UCSC Ensembl
Innerchr1:80309805..80403819hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3894015
hg1994015
hg1894015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv340n54
Supporting Variantsnssv718341, nssv718342
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546659
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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