A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979490



Internal ID18614692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32799205..32808021hg38UCSC Ensembl
Innerchr20:31387011..31395827hg19UCSC Ensembl
Innerchr20:30850672..30859488hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg388817
hg198817
hg188817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759683
SamplesHGDP00778
Known GenesDNMT3B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979490
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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