A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978411



Internal ID18613616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32053577..32085566hg38UCSC Ensembl
Innerchr17:30380596..30412585hg19UCSC Ensembl
Innerchr17:27404709..27436698hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3831990
hg1931990
hg1831990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2090134, nssv2090138, nssv2090141, nssv2090143, nssv2090135, nssv2090142, nssv2090140, nssv2090139, nssv2090136, nssv2090137
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)nsv978411
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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