A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2629n223



Internal ID22805597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92849751..92851015hg38UCSC Ensembl
chr15:93392981..93394245hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381265
hg191265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6583558, nsv6594866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2629n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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