A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982322



Internal ID18617517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94038022..94039417hg38UCSC Ensembl
Innerchr9:96800304..96801699hg19UCSC Ensembl
Innerchr9:95840125..95841520hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381396
hg191396
hg181396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559711, nssv2559717, nssv2559716, nssv2559715, nssv2559712, nssv2559709, nssv2559708, nssv2559714, nssv2559710, nssv2559713
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPTPDC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982322
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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