A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv184n223



Internal ID22803152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49368230..49430188hg38UCSC Ensembl
chr1:49833902..49895860hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3861959
hg1961959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6332881, nsv6317437
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv184n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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