A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230907



Internal ID20797947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111907648..111908205hg38UCSC Ensembl
chr12:112345452..112346009hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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