A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964074



Internal ID18599312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:94365068..94370972hg38UCSC Ensembl
Innerchr4:95286219..95292123hg19UCSC Ensembl
Innerchr4:95505242..95511146hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385905
hg195905
hg185905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2327270, nssv2327276, nssv2327275, nssv2327274, nssv2327271, nssv2327273, nssv2327269, nssv2327277, nssv2327278, nssv2327272
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)nsv964074
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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