A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3825n223



Internal ID22806793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32866860..36090731hg38UCSC Ensembl
chr2:33091927..36317874hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg383223872
hg193225948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6542569, nsv6548399
Samples
Known GenesFAM98A, LINC00486, LOC100271832, LTBP1, MYADML, RASGRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3825n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer