A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1030339



Internal ID15883525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52037296..52146437hg38UCSC Ensembl
Innerchr5:51333130..51442271hg19UCSC Ensembl
Innerchr5:51368887..51478028hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38109142
hg19109142
hg18109142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598154
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)nssv1030339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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