A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621032



Internal ID21813079
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 StatusS
Merged Variantsnsv6049729
Supporting Variants
Samples
Known GenesAPCDD1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621032
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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