A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226844



Internal ID20793884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:428014..744559hg38UCSC Ensembl
chr11:428014..744559hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38316546
hg19316546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591624
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)nssv18226844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0019


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