A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735372



Internal ID159038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56083034..56083219hg38UCSC Ensembl
chr5:55378861..55379046hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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