A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519771



Internal ID15100378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5460910..5464065hg38UCSC Ensembl
Innerchr9:5460910..5464065hg19UCSC Ensembl
Innerchr9:5450910..5454065hg18UCSC Ensembl
Innerchr9:5450910..5454065hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg383156
hg193156
hg183156
hg173156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661704, nssv675996, nssv676309, nssv688016, nssv659183, nssv681109, nssv691639, nssv658438
Samples
Known GenesCD274
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519771
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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