A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497656



Internal ID274682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123207954..123208502hg38UCSC Ensembl
chr11:123078662..123079210hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497656
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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