A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219995



Internal ID20787035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110140563..110140974hg38UCSC Ensembl
chr10:111900321..111900732hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219995
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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