A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234251



Internal ID20801291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19096132..19097424hg38UCSC Ensembl
chr12:19249066..19250358hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381293
hg191293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234251
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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