A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522929



Internal ID15450222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11430378..11535770hg38UCSC Ensembl
Innerchr20:11411026..11516418hg19UCSC Ensembl
Innerchr20:11359026..11464418hg18UCSC Ensembl
Innerchr20:11359026..11464418hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38105393
hg19105393
hg18105393
hg17105393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698592
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522929
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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