A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1032504



Internal ID15885690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:129166045..129218502hg38UCSC Ensembl
Innerchr5:128501738..128554195hg19UCSC Ensembl
Innerchr5:128529637..128582094hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3852458
hg1952458
hg1852458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599703
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)nssv1032504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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