A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525278



Internal ID15105885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240001219..240122324hg38UCSC Ensembl
Innerchr2:240940636..241061741hg19UCSC Ensembl
Innerchr2:240589309..240710414hg18UCSC Ensembl
Innerchr2:240660626..240781731hg17UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38121106
hg19121106
hg18121106
hg17121106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701381
Samples
Known GenesNDUFA10, OR6B2, OR6B3, PRR21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525278
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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