A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598654



Internal ID20971725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45769200..45769957hg38UCSC Ensembl
chr20:44397839..44398596hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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