A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972423



Internal ID18607639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94481483..94492314hg38UCSC Ensembl
Innerchr9:97243765..97254596hg19UCSC Ensembl
Innerchr9:96283586..96294417hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3810832
hg1910832
hg1810832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559208, nssv2559210, nssv2559204, nssv2559207, nssv2559201, nssv2559205, nssv2559203, nssv2559209, nssv2559202, nssv2559206
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)nsv972423
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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