A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520338



Internal ID20893699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67143533..67551977hg38UCSC Ensembl
chr18:64810770..65219214hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38408445
hg19408445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197584
Samples
Known GenesDSEL, LOC643542
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520338
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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