A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100393



Internal ID20667433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23825465..23885211hg38UCSC Ensembl
chr3:23866956..23926702hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3859747
hg1959747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358060
Supporting Variants
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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