A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051575



Internal ID102232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127524147..127524223hg38UCSC Ensembl
chr11:127394042..127394118hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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