A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590139



Internal ID20963210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38695377..38743385hg38UCSC Ensembl
chr18:36275341..36323349hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3848009
hg1948009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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