A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593431



Internal ID20966502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23122051..23123217hg38UCSC Ensembl
chr18:20702015..20703181hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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