A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961165



Internal ID18249725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3567351..3579402hg38UCSC Ensembl
Innerchr19:3567349..3579400hg19UCSC Ensembl
Innerchr19:3518349..3530400hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812052
hg1912052
hg1812052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2128387, nssv2128393, nssv2128389, nssv2128386, nssv2128388, nssv2128391, nssv2128390, nssv2128384, nssv2128392, nssv2128385
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHMG20B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961165
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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