A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587679



Internal ID20960750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54501395..54502605hg38UCSC Ensembl
chr18:52027765..52028975hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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