A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960803



Internal ID18249364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15949029..15949639hg38UCSC Ensembl
Innerchr19:16059839..16060449hg19UCSC Ensembl
Innerchr19:15920839..15921449hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38611
hg19611
hg18611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2138222, nssv2138216, nssv2138215, nssv2138221, nssv2138220, nssv2138218, nssv2138219, nssv2138217, nssv2138223, nssv2138214
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR10H4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960803
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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