A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598535



Internal ID20971606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20759302..20760094hg38UCSC Ensembl
chr20:20739945..20740737hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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