A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4972n223



Internal ID22807940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692348..107702300hg38UCSC Ensembl
chr3:107411195..107421147hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg389953
hg199953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6355599, nsv6370250
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4972n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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