A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973628



Internal ID18608843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42957654..42966031hg38UCSC Ensembl
Innerchr9:44005088..44013465hg19UCSC Ensembl
Innerchr9:43945084..43953461hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388378
hg198378
hg188378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2734052, nssv2734056, nssv2734051, nssv2734053, nssv2734054, nssv2734050, nssv2734055, nssv2734059, nssv2734058, nssv2734057
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)nsv973628
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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