A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597913



Internal ID20970984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33270431..33271604hg38UCSC Ensembl
chr21:34642736..34643909hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254033
Samples
Known GenesIL10RB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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