A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962273



Internal ID18597517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17241364..17243461hg38UCSC Ensembl
Innerchr17:17144678..17146775hg19UCSC Ensembl
Innerchr17:17085403..17087500hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382098
hg192098
hg182098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2082882, nssv2082875, nssv2082876, nssv2082878, nssv2082879, nssv2082877, nssv2082880, nssv2082881, nssv2082874, nssv2082883
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)nsv962273
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