A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524004



Internal ID15104611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47838171..48491735hg38UCSC Ensembl
Innerchr20:46466915..47119981hg19UCSC Ensembl
Innerchr20:45900322..46553388hg18UCSC Ensembl
Innerchr20:45900322..46553388hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38653565
hg19653067
hg18653067
hg17653067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699864
Samples
Known GenesLINC00494
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524004
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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