A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515713



Internal ID15443324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24429559..24445351hg38UCSC Ensembl
Innerchr20:24410195..24425987hg19UCSC Ensembl
Innerchr20:24358195..24373987hg18UCSC Ensembl
Innerchr20:24358195..24373987hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3815793
hg1915793
hg1815793
hg1715793
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661108, nssv664507, nssv670917, nssv668815, nssv662380
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515713
Frequency
Sample Size2026
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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