A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373841



Internal ID21031394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24394401..24435300hg38UCSC Ensembl
chr3:24435892..24476791hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3840900
hg1940900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4823n223
Supporting Variantsnssv18101031
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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