A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210030



Internal ID20777070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55466334..55466927hg38UCSC Ensembl
chr3:55500362..55500955hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364883
Supporting Variants
Samples
Known GenesWNT5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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