A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228675



Internal ID20795715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96071686..96072076hg38UCSC Ensembl
chr12:96465464..96465854hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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