A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534198



Internal ID310035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118401123..118401164hg38UCSC Ensembl
chr11:118271838..118271879hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053599
Samples
Known GenesLOC100131626
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534198
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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