A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960168



Internal ID18595421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26967715..26971674hg38UCSC Ensembl
Innerchr17:25294741..25298700hg19UCSC Ensembl
Innerchr17:22318868..22322827hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg383960
hg193960
hg183960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2654666, nssv2654667, nssv2654662, nssv2654671, nssv2654668, nssv2654669, nssv2654663, nssv2654664, nssv2654665, nssv2654670
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960168
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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