A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494837



Internal ID271967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67562615..67564980hg38UCSC Ensembl
chr11:67330086..67332451hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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