A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv385n206



Internal ID22755689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175568610..175628170hg38UCSC Ensembl
chr4:176489761..176549321hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3859561
hg1959561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5455123, nsv5473471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv385n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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