A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047048



Internal ID99206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58235908..58236023hg38UCSC Ensembl
chr11:58003380..58003495hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047048
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008742


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