A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027983



Internal ID21937326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25535894..25537046hg38UCSC Ensembl
chr11:25557440..25558592hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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