A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220878



Internal ID20787918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119179896..119180687hg38UCSC Ensembl
chr10:120939408..120940199hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220878
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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