A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043264



Internal ID96554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10346432..10349321hg38UCSC Ensembl
chr11:10367979..10370868hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496779
Supporting Variants
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043264
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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