A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044809



Internal ID21954089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62929003..62929695hg38UCSC Ensembl
chr20:61560355..61561047hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636121
Samples
Known GenesDIDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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