A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597581



Internal ID20970652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70060387..70083520hg38UCSC Ensembl
chr18:67727623..67750756hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3823134
hg1923134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244746
Samples
Known GenesRTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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