A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230826



Internal ID20797866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57327462..57328095hg38UCSC Ensembl
chr12:57721245..57721878hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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