A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524918



Internal ID15105525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26169872..26193167hg38UCSC Ensembl
Innerchr2:26392741..26416036hg19UCSC Ensembl
Innerchr2:26246245..26269540hg18UCSC Ensembl
Innerchr2:26304392..26327687hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3823296
hg1923296
hg1823296
hg1723296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700930
Samples
Known GenesGAREML, HADHA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524918
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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