A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594145



Internal ID20967216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50960039..50961703hg38UCSC Ensembl
chr18:48486409..48488073hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381665
hg191665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3365n223
Supporting Variantsnssv18244621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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