A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113756



Internal ID21297022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20059538..20064680hg38UCSC Ensembl
Innerchr17:19962851..19967993hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg385143
hg195143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098109
Samplessample80
Known GenesSPECC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113756
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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