A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366551



Internal ID21024104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23817319..23819129hg38UCSC Ensembl
chr3:23858810..23860620hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100392
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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