A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035437



Internal ID15888623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84569706..84640651hg38UCSC Ensembl
Innerchr5:83865524..83936469hg19UCSC Ensembl
Innerchr5:83901280..83972225hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3870946
hg1970946
hg1870946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598792
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)nssv1035437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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