A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223034



Internal ID20790074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57710781..57711620hg38UCSC Ensembl
chr12:58104564..58105403hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583833
Supporting Variants
Samples
Known GenesOS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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