A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022621



Internal ID21931964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59847874..59859206hg38UCSC Ensembl
chr11:59615347..59626679hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811333
hg1911333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584757
Samples
Known GenesTCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022621
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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