A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5258n223



Internal ID22808226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46887510..46888743hg38UCSC Ensembl
chr4:46889527..46890760hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6557137, nsv6564189
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5258n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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