A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562498



Internal ID20935569
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 StatusM
Merged Variants
Supporting Variantsnssv18280334
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)nsv6562498
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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