A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407218



Internal ID21064771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85854740..85867550hg38UCSC Ensembl
chr6:86564458..86577268hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3812811
hg1912811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407218
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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