A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364928



Internal ID21022481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23814660..23817280hg38UCSC Ensembl
chr3:23856151..23858771hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382621
hg192621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100391
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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