A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228518



Internal ID20795558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110309190..110309808hg38UCSC Ensembl
chr12:110746995..110747613hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577493
Supporting Variants
Samples
Known GenesATP2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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