A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562535



Internal ID335487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114319124..114322645hg38UCSC Ensembl
chr11:114189846..114193367hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg383522
hg193522
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562535
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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