A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057075



Internal ID21966308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50738107..50741992hg38UCSC Ensembl
chr20:49354644..49358529hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383886
hg193886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630573
Samples
Known GenesPARD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057075
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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