A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524362



Internal ID15104969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29089598..29155854hg38UCSC Ensembl
Innerchr15:29381801..29448057hg19UCSC Ensembl
Innerchr15:27169093..27235349hg18UCSC Ensembl
Innerchr15:27169093..27235349hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3866257
hg1966257
hg1866257
hg1766257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700273
Samples
Known GenesAPBA2, FAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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