A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255085



Internal ID20822125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43690612..45780509hg38UCSC Ensembl
chr21:45110493..47200423hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382089898
hg192089931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599512
Supporting Variants
Samples
Known GenesADARB1, AGPAT3, AIRE, C21orf2, C21orf33, C21orf67, C21orf90, COL18A1, COL18A1-AS1, COL18A1-AS2, CSTB, DNMT3L, FAM207A, ICOSLG, ITGB2, ITGB2-AS1, KRTAP10-1, KRTAP10-10, KRTAP10-11, KRTAP10-12, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, KRTAP12-1, KRTAP12-2, KRTAP12-3, KRTAP12-4, LINC00162, LINC00163, LINC00316, LOC284837, LOC642852, LRRC3, LRRC3-AS1, MIR6815, PDXK, PFKL, POFUT2, PTTG1IP, PWP2, RRP1, RRP1B, SLC19A1, SSR4P1, SUMO3, TRAPPC10, TRPM2, TSPEAR, TSPEAR-AS1, UBE2G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255085
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer