A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153282



Internal ID15877638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:593968..625555hg38UCSC Ensembl
Innerchr5:594083..625670hg19UCSC Ensembl
Innerchr5:647083..678670hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3831588
hg1931588
hg1831588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596708
Supporting Variants
SamplesHGDP01019
Known GenesCEP72, LOC100996325
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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