A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977075



Internal ID52110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167651079..167723765hg38UCSC Ensembl
chr5:167078084..167150770hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3872687
hg1972687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454301
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977075
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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