A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030418



Internal ID21939761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128219460..128230509hg38UCSC Ensembl
chr11:128089355..128100404hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811050
hg1911050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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