A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053371



Internal ID103429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123444028..123449797hg38UCSC Ensembl
chr11:123314736..123320505hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385770
hg195770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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