A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962301



Internal ID18597545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:29203763..29204263hg38UCSC Ensembl
Innerchr17:27530781..27531281hg19UCSC Ensembl
Innerchr17:24554907..24555407hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2089762, nssv2089757, nssv2089756, nssv2089760, nssv2089763, nssv2089758, nssv2089754, nssv2089759, nssv2089761, nssv2089755
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)nsv962301
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