A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280334



Internal ID20847374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20655689..27693631hg38UCSC Ensembl
chr9:20655688..27693629hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg387037943
hg197037942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562498
Supporting Variants
Samples
Known GenesC9orf53, C9orf72, CAAP1, CDKN2A, CDKN2B, CDKN2B-AS1, DMRTA1, ELAVL2, EQTN, FLJ35282, FOCAD, IFNA1, IFNA10, IFNA13, IFNA14, IFNA16, IFNA17, IFNA2, IFNA21, IFNA22P, IFNA4, IFNA5, IFNA6, IFNA7, IFNA8, IFNB1, IFNE, IFNK, IFNW1, IFT74, IZUMO3, KLHL9, LINC00032, LOC100506422, LRRC19, MIR31, MIR31HG, MIR491, MOB3B, MTAP, PLAA, PTPLAD2, TEK, TUSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280334
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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