A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961189



Internal ID18596435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14924669..14928046hg38UCSC Ensembl
Innerchr19:15035481..15038858hg19UCSC Ensembl
Innerchr19:14896481..14899858hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2136306, nssv2136314, nssv2136312, nssv2136311, nssv2136307, nssv2136309, nssv2136305, nssv2136310, nssv2136313, nssv2136308
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)nsv961189
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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