A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3816n223



Internal ID22806784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27648717..27649072hg38UCSC Ensembl
chr2:27871584..27871939hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6540320, nsv6544272
Samples
Known GenesGPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3816n223
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