A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506160



Internal ID282913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60713911..60714223hg38UCSC Ensembl
chr11:60481384..60481696hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045564
Samples
Known GenesMS4A8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506160
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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