A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5286n223



Internal ID22808254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62891701..64322157hg38UCSC Ensembl
chr4:63757419..65187875hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381430457
hg191430457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6392691, nsv6390931
Samples
Known GenesTECRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5286n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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