A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254155



Internal ID20821195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16563401..16564194hg38UCSC Ensembl
chr21:17935721..17936514hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597893
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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