A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598705



Internal ID20971776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58958652..58959539hg38UCSC Ensembl
chr20:57533707..57534594hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4501n223
Supporting Variantsnssv18253436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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