A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519797



Internal ID15100404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86084875..87238541hg38UCSC Ensembl
Innerchr15:86628106..87781772hg19UCSC Ensembl
Innerchr15:84429110..85582776hg18UCSC Ensembl
Innerchr15:84429110..85582776hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381153667
hg191153667
hg181153667
hg171153667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697057
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519797
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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