A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233224



Internal ID20800264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79720520..79720667hg38UCSC Ensembl
chr12:80114300..80114447hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233224
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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