A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599266



Internal ID20972337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44471979..44472693hg38UCSC Ensembl
chr20:43100619..43101333hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599266
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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