A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109406



Internal ID21282997
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 StatusS
Merged Variantsnsv3116377
Supporting Variants
Samplessample335
Known GenesHTR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109406
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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