A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972382



Internal ID18607598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63350216..63410891hg38UCSC Ensembl
Innerchr9:67305188..67365863hg19UCSC Ensembl
Innerchr9:66995008..67055683hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3860676
hg1960676
hg1860676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2548328, nssv2548323, nssv2548320, nssv2548322, nssv2548329, nssv2548324, nssv2548325, nssv2548327, nssv2548321, nssv2548326
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)nsv972382
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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