A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594450



Internal ID20967521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13710350..13711161hg38UCSC Ensembl
chr18:13710349..13711160hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243477
Samples
Known GenesFAM210A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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