A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594275



Internal ID20967346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10590151..10590463hg38UCSC Ensembl
chr18:10590148..10590460hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594275
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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