A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586025



Internal ID20959096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21893388..21894270hg38UCSC Ensembl
chr18:19473349..19474231hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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