A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962352



Internal ID18250910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60213764..60222118hg38UCSC Ensembl
Innerchr17:58291125..58299479hg19UCSC Ensembl
Innerchr17:55645907..55654261hg18UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg388355
hg198355
hg188355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2103811, nssv2103820, nssv2103816, nssv2103818, nssv2103819, nssv2103812, nssv2103813, nssv2103815, nssv2103814, nssv2103817
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUSP32
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962352
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer