A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517379



Internal ID15444672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11745912..12381912hg38UCSC Ensembl
Innerchr9:11745912..12381912hg19UCSC Ensembl
Innerchr9:11735912..12371912hg18UCSC Ensembl
Innerchr9:11735912..12371912hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38636001
hg19636001
hg18636001
hg17636001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700329, nssv666915, nssv664937, nssv679851, nssv670445, nssv656684, nssv688276, nssv695452, nssv699252, nssv673886, nssv662522, nssv681680, nssv671139, nssv657287, nssv702980, nssv662339, nssv658467, nssv666862, nssv659971, nssv683660, nssv678878, nssv674152, nssv671801, nssv688827, nssv687539, nssv654457, nssv702303, nssv678657, nssv681453, nssv657909, nssv686245, nssv652440, nssv702876, nssv692043, nssv677436, nssv702331, nssv686589, nssv673216, nssv668572, nssv694465, nssv705071, nssv658038, nssv699829, nssv662262, nssv678207, nssv692461, nssv663533, nssv700104, nssv675981, nssv651858, nssv704209, nssv699853, nssv659490, nssv658702, nssv684289, nssv687309, nssv696996, nssv674695, nssv681987, nssv702511, nssv678834, nssv676650, nssv697096, nssv667485, nssv684607, nssv680027, nssv700369, nssv656718, nssv682615, nssv683549, nssv671863, nssv700144, nssv697419, nssv678366, nssv681205, nssv693538, nssv677292, nssv681988, nssv693925
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517379
Frequency
Sample Size2026
Observed Gain0
Observed Loss79
Observed Complex0
Frequencyn/a


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