A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254044



Internal ID20821084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33464299..33464799hg38UCSC Ensembl
chr21:34836606..34837106hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596674
Supporting Variants
Samples
Known GenesTMEM50B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254044
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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