A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521543



Internal ID15448836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89405705..89405979hg38UCSC Ensembl
Innerchr15:89948936..89949210hg19UCSC Ensembl
Innerchr15:87749940..87750214hg18UCSC Ensembl
Innerchr15:87749940..87750214hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38275
hg19275
hg18275
hg17275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698159
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521543
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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