A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963009



Internal ID18598251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13155929..13160121hg38UCSC Ensembl
Innerchr19:13266743..13270935hg19UCSC Ensembl
Innerchr19:13127743..13131935hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg384193
hg194193
hg184193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2134826, nssv2134825, nssv2134820, nssv2134819, nssv2134821, nssv2134823, nssv2134824, nssv2134818, nssv2134827, nssv2134822
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963009
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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