A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116377



Internal ID21299643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:148568672..148571303hg38UCSC Ensembl
Innerchr5:147948235..147950866hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109406
Samplessample335
Known GenesHTR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116377
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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