A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980264



Internal ID18615464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144845502..144850683hg38UCSC Ensembl
Innerchr4:145766654..145771835hg19UCSC Ensembl
Innerchr4:145986104..145991285hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385182
hg195182
hg185182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2338405, nssv2338406, nssv2338413, nssv2338411, nssv2338407, nssv2338410, nssv2338409, nssv2338408, nssv2338414, nssv2338412
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)nsv980264
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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