A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598829



Internal ID20971900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33453174..33453904hg38UCSC Ensembl
chr21:34825481..34826211hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254043
Samples
Known GenesTMEM50B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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