A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594040



Internal ID20967111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38481545..38899482hg38UCSC Ensembl
chr18:36061509..36479446hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38417938
hg19417938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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