A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595147



Internal ID20968218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61929286..61931227hg38UCSC Ensembl
chr18:59596519..59598460hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595147
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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