A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960773



Internal ID18596020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2927338..2931838hg38UCSC Ensembl
Innerchr19:2927336..2931836hg19UCSC Ensembl
Innerchr19:2878336..2882836hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384501
hg194501
hg184501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2127407, nssv2127398, nssv2127405, nssv2127406, nssv2127399, nssv2127404, nssv2127400, nssv2127401, nssv2127403, nssv2127402
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)nsv960773
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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