A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598525



Internal ID20971596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63626801..63956899hg38UCSC Ensembl
chr20:62258154..62588252hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38330099
hg19330099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254090
Samples
Known GenesABHD16B, ARFRP1, DNAJC5, GMEB2, LIME1, MIR1914, MIR647, MIR941-1, MIR941-2, MIR941-3, MIR941-4, RTEL1, RTEL1-TNFRSF6B, SLC2A4RG, STMN3, TNFRSF6B, TPD52L2, UCKL1, UCKL1-AS1, ZBTB46, ZGPAT, ZNF512B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598525
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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