A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960836



Internal ID18596083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37864568..37879666hg38UCSC Ensembl
Innerchr19:38355208..38370306hg19UCSC Ensembl
Innerchr19:43047048..43062146hg18UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3815099
hg1915099
hg1815099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2147761, nssv2147760, nssv2147757, nssv2147755, nssv2147759, nssv2147754, nssv2147753, nssv2147756, nssv2147758, nssv2147752
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)nsv960836
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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