A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528937



Internal ID15456230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100689579..100763961hg38UCSC Ensembl
Innerchr15:101229784..101304166hg19UCSC Ensembl
Innerchr15:99047307..99121689hg18UCSC Ensembl
Innerchr15:99047307..99121689hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3874383
hg1974383
hg1874383
hg1774383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705628
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528937
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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