A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489310



Internal ID21146863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62610501..62652200hg38UCSC Ensembl
chr13:63184634..63226333hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489310
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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