A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255084



Internal ID20822124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43689244..45912414hg38UCSC Ensembl
chr21:45109125..47332328hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382223171
hg192223204
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599116
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, LOC100129027, LOC284837, LOC642852, LRRC3, LRRC3-AS1, MIR6815, PCBP3, 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)nssv18255084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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