A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295081



Internal ID20504299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17768362..17861561hg38UCSC Ensembl
chr12:17921296..18014495hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3893200
hg1993200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295081
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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