A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966381



Internal ID44909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32913607..32919780hg38UCSC Ensembl
chr5:32913713..32919886hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg386174
hg196174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460613
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966381
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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