A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596455



Internal ID20969526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71458374..71459846hg38UCSC Ensembl
chr18:69125610..69127082hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n223
Supporting Variantsnssv18244782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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