A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968596



Internal ID18603824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15361446..15363946hg38UCSC Ensembl
Innerchr9:15361444..15363944hg19UCSC Ensembl
Innerchr9:15351444..15353944hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382501
hg192501
hg182501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522820, nssv2522824, nssv2522815, nssv2522822, nssv2522817, nssv2522821, nssv2522823, nssv2522819, nssv2522816, nssv2522818
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)nsv968596
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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