A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026842



Internal ID16320798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20953320..21069254hg38UCSC Ensembl
Innerchr5:20953429..21069363hg19UCSC Ensembl
Innerchr5:20989186..21105120hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38115935
hg19115935
hg18115935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597435
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)nssv1026842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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