A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497097



Internal ID274153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24318174..24319949hg38UCSC Ensembl
chr11:24339720..24341495hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381776
hg191776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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