A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043319



Internal ID96589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11133648..11138971hg38UCSC Ensembl
chr11:11155195..11160518hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385324
hg195324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043319
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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