A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966267



Internal ID18601497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49486925..49524562hg38UCSC Ensembl
Innerchr4:49488942..49526579hg19UCSC Ensembl
Innerchr4:49183599..49221336hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3837638
hg1937638
hg1837738
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2318598, nssv2318595, nssv2318601, nssv2318593, nssv2318597, nssv2318594, nssv2318599, nssv2318592, nssv2318596, nssv2318600
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)nsv966267
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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