A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963358



Internal ID18598599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122660821..122666333hg38UCSC Ensembl
Innerchr3:122379668..122385180hg19UCSC Ensembl
Innerchr3:123862358..123867870hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg385513
hg195513
hg185513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2296043, nssv2296042, nssv2296036, nssv2296035, nssv2296039, nssv2296044, nssv2296040, nssv2296037, nssv2296041, nssv2296038
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)nsv963358
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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