A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964091



Internal ID18599329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119334187..119369796hg38UCSC Ensembl
Innerchr4:120255342..120290951hg19UCSC Ensembl
Innerchr4:120474790..120510399hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3835610
hg1935610
hg1835610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2334572, nssv2334569, nssv2334567, nssv2334563, nssv2334570, nssv2334566, nssv2334564, nssv2334571, nssv2334568, nssv2334565
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)nsv964091
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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