A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522831



Internal ID15450124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37251359..37254547hg38UCSC Ensembl
Innerchr15:37543560..37546748hg19UCSC Ensembl
Innerchr15:35330852..35334040hg18UCSC Ensembl
Innerchr15:35330852..35334040hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383189
hg193189
hg183189
hg173189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698481
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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