A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226856



Internal ID20793896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110762697..110767700hg38UCSC Ensembl
chr10:112522455..112527458hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385004
hg195004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579314
Supporting Variants
Samples
Known GenesRBM20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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