A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254439



Internal ID20821479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10584617..10585207hg38UCSC Ensembl
chr21:10927250..10927840hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598609
Supporting Variants
Samples
Known GenesTPTE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254439
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00114


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