A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946065



Internal ID18592915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90286641..90298229hg38UCSC Ensembl
Innerchr1:90752199..90763787hg19UCSC Ensembl
Innerchr1:90524787..90536375hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3811589
hg1911589
hg1811589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1776283, nssv1776289, nssv1776287, nssv1776292, nssv1776284, nssv1776286, nssv1776291, nssv1776285, nssv1776288, nssv1776290
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)nsv946065
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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