A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978514



Internal ID53053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167014390..167014478hg38UCSC Ensembl
chr5:166441395..166441483hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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