A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047952



Internal ID21957185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1002556..1150184hg38UCSC Ensembl
chr20:983199..1130827hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38147629
hg19147629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633406
Samples
Known GenesPSMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047952
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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