A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718341



Internal ID16012297
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 StatusS
Merged Variantsnsv546659
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv718341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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