A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv881n223



Internal ID22803849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104540873..104676112hg38UCSC Ensembl
chr10:106300631..106435870hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38135240
hg19135240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6575962, nsv6581839, nsv6591393
Samples
Known GenesSORCS3, SORCS3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv881n223
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