A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520963



Internal ID15101570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160216207..160217044hg38UCSC Ensembl
Innerchr6:160637239..160638076hg19UCSC Ensembl
Innerchr6:160557229..160558066hg18UCSC Ensembl
Innerchr6:160607650..160608487hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
hg17838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689591, nssv678874
Samples
Known GenesSLC22A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520963
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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