A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228868



Internal ID20795908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94550848..94551903hg38UCSC Ensembl
chr10:96310605..96311660hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584756
Supporting Variants
Samples
Known GenesHELLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228868
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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