A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5585n223



Internal ID22808553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:239093..1858568hg38UCSC Ensembl
chr5:239208..1858682hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381619476
hg191619475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6569936, nsv6559982, nsv6569163, nsv6563131, nsv6560118, nsv6575170, nsv6565030, nsv6567816, nsv6563484, nsv6559864
Samples
Known GenesAHRR, BRD9, C5orf55, CEP72, CLPTM1L, EXOC3, LOC100506688, LOC100996325, LOC101929034, LOC102467073, LOC728613, LPCAT1, MIR4277, MIR4456, MIR4457, MIR4635, MIR6075, MRPL36, NDUFS6, NKD2, PDCD6, PP7080, SDHA, SDHAP3, SLC12A7, SLC6A18, SLC6A19, SLC6A3, SLC9A3, TERT, TPPP, TRIP13, ZDHHC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5585n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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