A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100366



Internal ID20667406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23423297..23424010hg38UCSC Ensembl
chr3:23464788..23465501hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372622
Supporting Variants
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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