A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218809



Internal ID20785849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:427925..744841hg38UCSC Ensembl
chr11:427925..744841hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38316917
hg19316917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588565
Supporting Variants
Samples
Known GenesANO9, C11orf35, CDHR5, DEAF1, DRD4, EPS8L2, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PTDSS2, RASSF7, RNH1, SCT, TMEM80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00204


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