A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13n199



Internal ID22802899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26570660..27316835hg38UCSC Ensembl
chr10:26859589..27605764hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38746176
hg19746176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4755997, nsv4756180
Samples
Known GenesABI1, ACBD5, ANKRD26, LINC00202-1, LINC00202-2, LINC00264, LRRC37A6P, MASTL, PDSS1, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv13n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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