A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236526



Internal ID20803566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93309060..93309515hg38UCSC Ensembl
chr12:93702836..93703291hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583107
Supporting Variants
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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