A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500559



Internal ID277492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19725461..19730408hg38UCSC Ensembl
chr11:19747007..19751954hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384948
hg194948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044745
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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