A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5338n223



Internal ID22808306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74988701..74991891hg38UCSC Ensembl
chr4:75913911..75917101hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383191
hg193191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6391123, nsv6380231
Samples
Known GenesPARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5338n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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