A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599557



Internal ID20972628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63925378..63925498hg38UCSC Ensembl
chr20:62556731..62556851hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254095
Samples
Known GenesDNAJC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599557
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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