A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524593



Internal ID15451886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10967187..10968760hg38UCSC Ensembl
Innerchr5:10967299..10968872hg19UCSC Ensembl
Innerchr5:11020299..11021872hg18UCSC Ensembl
Innerchr5:11020299..11021872hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381574
hg191574
hg181574
hg171574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700552
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524593
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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