A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029878



Internal ID21939221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120083047..120083126hg38UCSC Ensembl
chr11:119953756..119953835hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029878
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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