A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2583n223



Internal ID22805551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75225241..75762978hg38UCSC Ensembl
chr15:75517582..76055319hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38537738
hg19537738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6588320, nsv6589853, nsv6579598
Samples
Known GenesCOMMD4, CSPG4, DNM1P35, GOLGA6C, GOLGA6D, IMP3, MAN2C1, MIR4313, MIR631, NEIL1, ODF3L1, PTPN9, SIN3A, SNUPN, SNX33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2583n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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