A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593914



Internal ID20966985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12670325..12670429hg38UCSC Ensembl
chr18:12670324..12670428hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243451
Samples
Known GenesCEP76, PSMG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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