A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2626n223



Internal ID22805594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90589101..90590265hg38UCSC Ensembl
chr15:91132333..91133497hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585213, nsv6585227
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2626n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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