A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512982



Internal ID289520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134934426..135024674hg38UCSC Ensembl
chr11:134804320..134894568hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3890249
hg1990249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512982
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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