A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977498



Internal ID18612704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92025490..92028159hg38UCSC Ensembl
Innerchr14:92491834..92494503hg19UCSC Ensembl
Innerchr14:91561587..91564256hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg382670
hg192670
hg182670
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1996060, nssv1996055, nssv1996056, nssv1996054, nssv1996059, nssv1996062, nssv1996058, nssv1996057, nssv1996063, nssv1996061
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTRIP11
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977498
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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