A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1032255



Internal ID15885441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:128000341..128012123hg38UCSC Ensembl
Innerchr5:127336033..127347815hg19UCSC Ensembl
Innerchr5:127363932..127375714hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3811783
hg1911783
hg1811783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599668
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)nssv1032255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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