A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976519



Internal ID51735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162706511..162716020hg38UCSC Ensembl
chr5:162133517..162143026hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg389510
hg199510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976519
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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