A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966015



Internal ID44666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55559811..55560124hg38UCSC Ensembl
chr5:54855639..54855952hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966015
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011871


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