A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5913n223



Internal ID22808881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119215476..119216010hg38UCSC Ensembl
chr5:118551171..118551705hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6556543, nsv6574552
Samples
Known GenesDMXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5913n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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