A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv260n223



Internal ID22803228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89009201..89013300hg38UCSC Ensembl
chr1:89474884..89478983hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6332601, nsv6322982
Samples
Known GenesGBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv260n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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