A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599991



Internal ID20973062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49933118..49934654hg38UCSC Ensembl
chr20:48549655..48551191hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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