A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972296



Internal ID18607512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14978871..14982047hg38UCSC Ensembl
Innerchr9:14978869..14982045hg19UCSC Ensembl
Innerchr9:14968869..14972045hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg383177
hg193177
hg183177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2523261, nssv2523263, nssv2523260, nssv2523255, nssv2523254, nssv2523259, nssv2523257, nssv2523262, nssv2523256, nssv2523258
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)nsv972296
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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