A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598853



Internal ID20971924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32705528..32706043hg38UCSC Ensembl
chr20:31293330..31293845hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251746
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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