A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968610



Internal ID18603838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35505261..35509524hg38UCSC Ensembl
Innerchr9:35505258..35509521hg19UCSC Ensembl
Innerchr9:35495258..35499521hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384264
hg194264
hg184264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527830, nssv2527831, nssv2527824, nssv2527822, nssv2527828, nssv2527827, nssv2527825, nssv2527823, nssv2527826, nssv2527829
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRUSC2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968610
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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