A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224581



Internal ID20791621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116661290..116662910hg38UCSC Ensembl
chr10:118420801..118422421hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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