A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960456



Internal ID18595707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28466665..28469275hg38UCSC Ensembl
Innerchr17:26793683..26796293hg19UCSC Ensembl
Innerchr17:23817810..23820420hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382611
hg192611
hg182611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2088558, nssv2088559, nssv2088560, nssv2089357, nssv2089358, nssv2088562, nssv2088563, nssv2089359, nssv2088561, nssv2089356
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)nsv960456
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