A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395942



Internal ID21053495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65589243..65601296hg38UCSC Ensembl
chr5:64885070..64897123hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3812054
hg1912054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214828
Samples
Known GenesTRIM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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