A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519775



Internal ID15100382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133265612..133273564hg38UCSC Ensembl
Innerchr8:134277855..134285807hg19UCSC Ensembl
Innerchr8:134347037..134354989hg18UCSC Ensembl
Innerchr8:134347037..134354989hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg387953
hg197953
hg187953
hg177953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658465, nssv658520
Samples
Known GenesNDRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519775
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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