A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364787



Internal ID21022340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137990378..138008195hg38UCSC Ensembl
chr3:137709220..137727037hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3817818
hg1917818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209612
Samples
Known GenesCLDN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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