A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502286



Internal ID279159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11754793..11760299hg38UCSC Ensembl
chr11:11776340..11781846hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385507
hg195507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502286
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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