A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1030337



Internal ID15883523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52037296..52129677hg38UCSC Ensembl
Innerchr5:51333130..51425511hg19UCSC Ensembl
Innerchr5:51368887..51461268hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3892382
hg1992382
hg1892382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598152
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)nssv1030337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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