A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522247



Internal ID15102854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39210097..39248129hg38UCSC Ensembl
Innerchr20:37838740..37876772hg19UCSC Ensembl
Innerchr20:37272154..37310186hg18UCSC Ensembl
Innerchr20:37272154..37310186hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3838033
hg1938033
hg1838033
hg1738033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695027
Samples
Known GenesLOC339568
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522247
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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