A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658520



Internal ID15048486
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519775
Supporting Variants
Samples
Known GenesNDRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658520
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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