A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968605



Internal ID18603833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33674548..33676251hg38UCSC Ensembl
Innerchr9:33674546..33676249hg19UCSC Ensembl
Innerchr9:33664546..33666249hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381704
hg191704
hg181704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527035, nssv2527038, nssv2527030, nssv2527037, nssv2527031, nssv2527039, nssv2527036, nssv2527033, nssv2527034, nssv2527032
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPTENP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968605
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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