A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223974



Internal ID20791014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25847102..25847819hg38UCSC Ensembl
chr12:26000036..26000752hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38718
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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