A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112234



Internal ID21295500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35487629..35490227hg38UCSC Ensembl
Innerchr17:33814648..33817246hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097681
Samplessample226
Known GenesSLFN12L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112234
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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