A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116077



Internal ID21299343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113549641..113553654hg38UCSC Ensembl
Innerchr5:112885338..112889351hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097332
Samplessample90
Known GenesYTHDC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116077
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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