A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535061



Internal ID310775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118828548..118828586hg38UCSC Ensembl
chr11:118699257..118699295hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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