A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517389



Internal ID15444682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87256693..87320484hg38UCSC Ensembl
Innerchr15:87799924..87863715hg19UCSC Ensembl
Innerchr15:85600928..85664719hg18UCSC Ensembl
Innerchr15:85600928..85664719hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3863792
hg1963792
hg1863792
hg1763792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669708, nssv685332, nssv683278, nssv666366, nssv651880, nssv656206, nssv669475, nssv671984, nssv661835, nssv657737, nssv653114, nssv666099, nssv652279, nssv686381, nssv658751, nssv664480, nssv677590, nssv660509, nssv671517, nssv692729, nssv679949, nssv666029, nssv659033, nssv681828
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517389
Frequency
Sample Size2026
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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