A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506993



Internal ID283723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63250190..63250414hg38UCSC Ensembl
chr11:63017662..63017886hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047926
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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