A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227176



Internal ID20794216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50190144..50191000hg38UCSC Ensembl
chr12:50583927..50584783hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587719
Supporting Variants
Samples
Known GenesLIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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