A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598807



Internal ID20971878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3542924..3543709hg38UCSC Ensembl
chr20:3523571..3524356hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252494
Samples
Known GenesATRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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