A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978833



Internal ID18614036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49275065..49284171hg38UCSC Ensembl
Innerchr19:49778322..49787428hg19UCSC Ensembl
Innerchr19:54470134..54479240hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg389107
hg199107
hg189107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2153878, nssv2153875, nssv2153871, nssv2153873, nssv2153874, nssv2153872, nssv2153869, nssv2153876, nssv2153877, nssv2153870
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)nsv978833
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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