A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233369



Internal ID20800409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95007214..95007722hg38UCSC Ensembl
chr12:95400990..95401498hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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