A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522887



Internal ID15450180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24772048..24777800hg38UCSC Ensembl
Innerchr15:25017195..25022947hg19UCSC Ensembl
Innerchr15:22568288..22574040hg18UCSC Ensembl
Innerchr15:22568288..22574040hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385753
hg195753
hg185753
hg175753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698545
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522887
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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