A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101131



Internal ID20668171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25630074..25630481hg38UCSC Ensembl
chr3:25671565..25671972hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365011
Supporting Variants
Samples
Known GenesTOP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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