A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960088



Internal ID18248655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31033387..31051069hg38UCSC Ensembl
Innerchr17:29360405..29378087hg19UCSC Ensembl
Innerchr17:26384531..26402213hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3817683
hg1917683
hg1817683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2089431, nssv2089434, nssv2089425, nssv2089430, nssv2089432, nssv2089429, nssv2089428, nssv2089433, nssv2089426, nssv2089427
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)nsv960088
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