A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960804



Internal ID18596051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16099920..16102759hg38UCSC Ensembl
Innerchr19:16210730..16213569hg19UCSC Ensembl
Innerchr19:16071730..16074569hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382840
hg192840
hg182840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2136739, nssv2136738, nssv2136743, nssv2136744, nssv2136736, nssv2136740, nssv2136745, nssv2136742, nssv2136737, nssv2136741
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTPM4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960804
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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