A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223249



Internal ID20790289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8607902..8608407hg38UCSC Ensembl
chr12:8760498..8761003hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580726
Supporting Variants
Samples
Known GenesAICDA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223249
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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