A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224693



Internal ID20791733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69344367..69348166hg38UCSC Ensembl
chr12:69738147..69741946hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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