A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513887



Internal ID290396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1654034..1657382hg38UCSC Ensembl
chr11:1675264..1678612hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383349
hg193349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040573
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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