A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051643



Internal ID102277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128236159..128238298hg38UCSC Ensembl
chr11:128106054..128108193hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051643
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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