A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3863n223



Internal ID22806831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:50522770..50524406hg38UCSC Ensembl
chr2:50749908..50751544hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg381637
hg191637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6542191, nsv6544890
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3863n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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