A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596478



Internal ID20969549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63923420..63923605hg38UCSC Ensembl
chr20:62554773..62554958hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254093
Samples
Known GenesDNAJC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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