A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594952



Internal ID20968023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46241427..46242183hg38UCSC Ensembl
chr18:43821393..43822149hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246885
Samples
Known GenesC18orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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