A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501375



Internal ID278274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91761839..91808772hg38UCSC Ensembl
chr11:91495005..91541938hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3846934
hg1946934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501375
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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