A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718355



Internal ID16012311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80793452..80876209hg38UCSC Ensembl
Innerchr1:81259137..81341894hg19UCSC Ensembl
Innerchr1:81031725..81114482hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3882758
hg1982758
hg1882758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546670
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)nssv718355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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