A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513906



Internal ID290415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18076010..18078566hg38UCSC Ensembl
chr11:18097557..18100113hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382557
hg192557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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