A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234219



Internal ID20801259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87741593..87743898hg38UCSC Ensembl
chr10:89501350..89503655hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590108
Supporting Variants
Samples
Known GenesPAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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