A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965970



Internal ID44634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53726815..53734180hg38UCSC Ensembl
chr5:53022645..53030010hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg387366
hg197366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965970
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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