A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv717526



Internal ID16011482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72490354..72576196hg38UCSC Ensembl
Innerchr1:72956037..73041879hg19UCSC Ensembl
Innerchr1:72728625..72814467hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3885843
hg1985843
hg1885843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546563
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)nssv717526
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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