A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965784



Internal ID18601014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160740271..160741362hg38UCSC Ensembl
Innerchr6:161161303..161162394hg19UCSC Ensembl
Innerchr6:161081293..161082384hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429760, nssv2429758, nssv2429753, nssv2429756, nssv2429759, nssv2429754, nssv2429751, nssv2429757, nssv2429755, nssv2429752
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965784
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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