A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963016



Internal ID18598258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17588932..17591447hg38UCSC Ensembl
Innerchr19:17699741..17702256hg19UCSC Ensembl
Innerchr19:17560741..17563256hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382516
hg192516
hg182516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2136938, nssv2136937, nssv2136935, nssv2136933, nssv2136936, nssv2136932, nssv2136939, nssv2136934, nssv2136930, nssv2136931
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)nsv963016
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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