A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576143



Internal ID20949214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26392673..26393184hg38UCSC Ensembl
chr18:23972637..23973148hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576143
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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