A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229560



Internal ID20796600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69184323..69185742hg38UCSC Ensembl
chr10:70944079..70945498hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579902
Supporting Variants
Samples
Known GenesSUPV3L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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