A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718345



Internal ID16012301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80343349..80405007hg38UCSC Ensembl
Innerchr1:80809034..80870692hg19UCSC Ensembl
Innerchr1:80581622..80643280hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3861659
hg1961659
hg1861659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546662
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)nssv718345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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