A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735442



Internal ID159108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146483820..146486058hg38UCSC Ensembl
chr5:145863383..145865621hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470782
Supporting Variants
Samples
Known GenesTCERG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735442
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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