A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596857



Internal ID20969928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59053939..59055230hg38UCSC Ensembl
chr20:57628994..57630285hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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