A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224122



Internal ID20791162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896665..46915975hg38UCSC Ensembl
chr12:47290448..47309758hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819311
hg1919311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.05205


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