A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045066



Internal ID21954336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6117690..6117801hg38UCSC Ensembl
chr20:6098337..6098448hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631541
Samples
Known GenesFERMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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