A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528887



Internal ID15456180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37251359..37268588hg38UCSC Ensembl
Innerchr15:37543560..37560789hg19UCSC Ensembl
Innerchr15:35330852..35348081hg18UCSC Ensembl
Innerchr15:35330852..35348081hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3817230
hg1917230
hg1817230
hg1717230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705570
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528887
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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