A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972443



Internal ID18260973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113446450..113448884hg38UCSC Ensembl
Innerchr9:116208730..116211164hg19UCSC Ensembl
Innerchr9:115248551..115250985hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382435
hg192435
hg182435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565241, nssv2565247, nssv2565248, nssv2565243, nssv2565242, nssv2565244, nssv2565239, nssv2565245, nssv2565240, nssv2565246
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesRGS3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972443
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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