A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281393



Internal ID20848433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90743255..92932434hg38UCSC Ensembl
chr9:93505537..95694716hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382189180
hg192189180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556848
Supporting Variants
Samples
Known GenesANKRD19P, ASPN, AUH, BICD2, CENPP, ECM2, IARS, IPPK, LINC00475, LOC100128076, LOC100128361, LOC100129316, MIR3651, MIR3910-1, MIR3910-2, MIR4670, NFIL3, NOL8, OGN, OMD, ROR2, SNORA84, SPTLC1, SYK, ZNF484
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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