A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253740



Internal ID20820780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23574238..25319063hg38UCSC Ensembl
chr22:23916425..25715030hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381744826
hg191798606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599715
Supporting Variants
Samples
Known GenesADORA2A, ADORA2A-AS1, BCRP3, C22orf15, C22orf43, CABIN1, CHCHD10, CRYBB2, CRYBB3, DDT, DDTL, DERL3, FAM211B, GGT1, GGT5, GSTT1, GSTT2, GSTT2B, GSTTP1, GSTTP2, GUCD1, GUSBP11, IGLL1, IGLL3P, KIAA1671, LOC100128531, LOC284889, LOC391322, MIF, MMP11, PIWIL3, POM121L10P, POM121L9P, RGL4, SGSM1, SLC2A11, SMARCB1, SNRPD3, SPECC1L, SPECC1L-ADORA2A, SUSD2, TMEM211, TOP1P2, UPB1, VPREB3, ZNF70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253740
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00037


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