A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521395



Internal ID20894756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24805701..24836400hg38UCSC Ensembl
chr20:24786337..24817036hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3830700
hg1930700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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