A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526163



Internal ID15106770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175368755..176024960hg38UCSC Ensembl
Innerchr3:175086544..175742748hg19UCSC Ensembl
Innerchr3:176569238..177225442hg18UCSC Ensembl
Innerchr3:176569246..177225450hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38656206
hg19656205
hg18656205
hg17656205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702422
Samples
Known GenesMIR4789, MIR548AY, NAALADL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526163
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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