A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4892n223



Internal ID22807860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62509901..62548600hg38UCSC Ensembl
chr3:62495576..62534275hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3838700
hg1938700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6356231, nsv6363544, nsv6374174
Samples
Known GenesCADPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4892n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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