A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232002



Internal ID20799042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104948936..104949595hg38UCSC Ensembl
chr12:105342714..105343373hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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