A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1762n223



Internal ID22804730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19190117..21274519hg38UCSC Ensembl
chr13:19764257..21848658hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382084403
hg192084402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584192, nsv6584962, nsv6595178
Samples
Known GenesANKRD26P3, CRYL1, GJA3, GJB2, GJB6, IFT88, IL17D, LATS2, LINC00367, LINC00421, MIR4499, MPHOSPH8, MRP63, N6AMT2, PSPC1, SAP18, SKA3, TPTE2, XPO4, ZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1762n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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