A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598060



Internal ID20971131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56883967..56887313hg38UCSC Ensembl
chr20:55459023..55462369hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg383347
hg193347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598060
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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