A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv514n209



Internal ID22826589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19344229..24542503hg38UCSC Ensembl
chr13:19918369..25116641hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg385198275
hg195198273
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5978990, nsv5969193
Samples
Known GenesANKRD20A19P, ANKRD26P3, BASP1P1, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, CRYL1, FGF9, GJA3, GJB2, GJB6, IFT88, IL17D, LATS2, LINC00327, LINC00367, LINC00421, LINC00424, LINC00539, LINC00540, MICU2, MIPEP, MIPEPP3, MIR2276, MIR4499, MPHOSPH8, MRP63, N6AMT2, PARP4, PSPC1, SACS, SACS-AS1, SAP18, SGCG, SKA3, SPATA13, SPATA13-AS1, TNFRSF19, TPTE2, XPO4, ZDHHC20, ZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv514n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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