A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960800



Internal ID18596047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15877508..15892879hg38UCSC Ensembl
Innerchr19:15988318..16003689hg19UCSC Ensembl
Innerchr19:15849318..15864689hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3815372
hg1915372
hg1815372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2137098, nssv2137106, nssv2137101, nssv2137097, nssv2137099, nssv2137105, nssv2137102, nssv2137103, nssv2137104, nssv2137100
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYP4F2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960800
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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