A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965848



Internal ID18601078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4629402..4630917hg38UCSC Ensembl
Innerchr20:4610048..4611563hg19UCSC Ensembl
Innerchr20:4558048..4559563hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381516
hg191516
hg181516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2226808, nssv2226809, nssv2226807, nssv2226810, nssv2226811, nssv2226812, nssv2226813, nssv2226805, nssv2226804, nssv2226806
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965848
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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