A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485088



Internal ID21142641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56721201..56769300hg38UCSC Ensembl
chr13:57295335..57343434hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3848100
hg1948100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1847n223
Supporting Variantsnssv18183559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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