A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526483



Internal ID15453776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39151340..39172298hg38UCSC Ensembl
Innerchr15:39443541..39464499hg19UCSC Ensembl
Innerchr15:37230833..37251791hg18UCSC Ensembl
Innerchr15:37230833..37251791hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3820959
hg1920959
hg1820959
hg1720959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702792
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526483
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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