A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485979



Internal ID21143532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85749741..85758581hg38UCSC Ensembl
chr13:86323876..86332716hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388841
hg198841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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