A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503118



Internal ID279960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25102401..25283223hg38UCSC Ensembl
chr11:25123947..25304769hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38180823
hg19180823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503118
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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