A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511068



Internal ID287669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25615567..25740451hg38UCSC Ensembl
chr11:25637113..25761998hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38124885
hg19124886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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