A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963057



Internal ID18251613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43354318..43360076hg38UCSC Ensembl
Innerchr19:43858470..43864228hg19UCSC Ensembl
Innerchr19:48550310..48556068hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg385759
hg195759
hg185759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2152060, nssv2152059, nssv2152066, nssv2152061, nssv2152058, nssv2152063, nssv2152065, nssv2152057, nssv2152064, nssv2152062
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCD177
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963057
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer