A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525689



Internal ID15106296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60448642..60531218hg38UCSC Ensembl
Innerchr15:60740841..60823417hg19UCSC Ensembl
Innerchr15:58528133..58610709hg18UCSC Ensembl
Innerchr15:58528133..58610709hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3882577
hg1982577
hg1882577
hg1782577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701847
Samples
Known GenesNARG2, RORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525689
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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