A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598651



Internal ID20971722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33533644..33534397hg38UCSC Ensembl
chr21:34905950..34906703hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4592n223
Supporting Variantsnssv18254051
Samples
Known GenesGART
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598651
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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