A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978351



Internal ID18613556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3419040..3421505hg38UCSC Ensembl
Innerchr17:3322334..3324799hg19UCSC Ensembl
Innerchr17:3269084..3271549hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg382466
hg192466
hg182466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2073255, nssv2073257, nssv2073258, nssv2073252, nssv2073259, nssv2073256, nssv2073250, nssv2073253, nssv2073251, nssv2073254
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR3A3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978351
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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