A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978776



Internal ID18613979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14249823..14255661hg38UCSC Ensembl
Innerchr19:14360635..14366473hg19UCSC Ensembl
Innerchr19:14221635..14227473hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385839
hg195839
hg185839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2134496, nssv2134494, nssv2134493, nssv2134499, nssv2134498, nssv2134500, nssv2134495, nssv2134491, nssv2134497, nssv2134492
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)nsv978776
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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