A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981422



Internal ID18616619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138294708..138304683hg38UCSC Ensembl
Innerchr16:90252770..90263991hg19UCSC Ensembl
Innerchr7:34762..45983hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg389976
hg1911222
hg1811222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2708742, nssv2708735, nssv2708743, nssv2708744, nssv2708736, nssv2708741, nssv2708737, nssv2708740, nssv2708739, nssv2708738
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981422
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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