A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281069



Internal ID20848109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77399209..87276767hg38UCSC Ensembl
chr9:80014125..89891682hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389877559
hg199877558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568042
Supporting Variants
Samples
Known GenesAGTPBP1, C9orf153, C9orf170, C9orf64, CEP78, FRMD3, GAS1, GKAP1, GNA14, GNAQ, GOLM1, HNRNPK, IDNK, ISCA1, KIF27, LOC100506834, LOC101927450, LOC101927502, LOC389765, LOC440173, LOC494127, MIR7-1, NAA35, NTRK2, PSAT1, RASEF, RMI1, SLC28A3, SPATA31D1, SPATA31D3, SPATA31D4, SPATA31D5P, TLE1, TLE4, UBQLN1, VPS13A, ZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00493


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