A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968597



Internal ID18603825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15522709..15527789hg38UCSC Ensembl
Innerchr9:15522707..15527787hg19UCSC Ensembl
Innerchr9:15512707..15517787hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg385081
hg195081
hg185081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522913, nssv2522914, nssv2522912, nssv2522920, nssv2522916, nssv2522915, nssv2522919, nssv2522921, nssv2522918, nssv2522917
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)nsv968597
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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