A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv158n223



Internal ID22803126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35510714..35512288hg38UCSC Ensembl
chr1:35976315..35977889hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6541604, nsv6550069
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv158n223
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