A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960862



Internal ID18596109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52277054..52282293hg38UCSC Ensembl
Innerchr19:52780307..52785546hg19UCSC Ensembl
Innerchr19:57472119..57477358hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385240
hg195240
hg185240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2155500, nssv2155496, nssv2155502, nssv2155494, nssv2155497, nssv2155498, nssv2155495, nssv2155493, nssv2155501, nssv2155499
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR643, ZNF766
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960862
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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