A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049729



Internal ID21958962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58519945..58520301hg38UCSC Ensembl
chr20:57095001..57095357hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621032
Samples
Known GenesAPCDD1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049729
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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