A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152991



Internal ID15854956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3678544..3700054hg38UCSC Ensembl
Innerchr5:3678658..3700168hg19UCSC Ensembl
Innerchr5:3731658..3753168hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3821511
hg1921511
hg1821511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596928
Supporting Variants
Samples1780862401_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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