A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972343



Internal ID18607559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66184023..66197604hg38UCSC Ensembl
Innerchr9:43164601..43178182hg19UCSC Ensembl
Innerchr9:43154597..43168178hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813582
hg1913582
hg1813582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2538188, nssv2538191, nssv2538194, nssv2538187, nssv2538196, nssv2538193, nssv2538192, nssv2538190, nssv2538189, nssv2538195
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)nsv972343
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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