A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021420



Internal ID21930763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111452883..111454262hg38UCSC Ensembl
chr11:111323608..111324987hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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