A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063553



Internal ID19152772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52310551..52419013hg38UCSC Ensembl
Innerchr20:50927090..51035552hg19UCSC Ensembl
Innerchr20:50360497..50468959hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38108463
hg19108463
hg18108463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731365
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063553
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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