A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116763



Internal ID21300029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66013031..66018388hg38UCSC Ensembl
Innerchr17:64009149..64014506hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097604
Samplessample194
Known GenesCEP112
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116763
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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