A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254463



Internal ID20821503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41196003..41197075hg38UCSC Ensembl
chr21:42567930..42569002hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597060
Supporting Variants
Samples
Known GenesBACE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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