A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279926



Internal ID20846966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12646715..21082031hg38UCSC Ensembl
chr9:12646715..21082030hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg388435317
hg198435316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564848
Supporting Variants
Samples
Known GenesACER2, ADAMTSL1, BNC2, C9orf92, CCDC171, CER1, CNTLN, DENND4C, FAM154A, FLJ41200, FOCAD, FREM1, HAUS6, IFNB1, LINC00583, LOC389705, LURAP1L, MIR3152, MIR4473, MIR4474, MIR491, MLLT3, MPDZ, NFIB, PLIN2, PSIP1, PTPLAD2, RPS6, RRAGA, SCARNA8, SH3GL2, SLC24A2, SNAPC3, TTC39B, TYRP1, ZDHHC21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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