A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519572



Internal ID15446865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39800269..39808427hg38UCSC Ensembl
Innerchr20:38428911..38437069hg19UCSC Ensembl
Innerchr20:37862325..37870483hg18UCSC Ensembl
Innerchr20:37862325..37870483hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg388159
hg198159
hg188159
hg178159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656921, nssv686450
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519572
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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