A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248052



Internal ID20815092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168546350..168574211hg38UCSC Ensembl
chr1:168515588..168543449hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3827862
hg1927862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248052
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00275


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