A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231451



Internal ID20798491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30610411..30611676hg38UCSC Ensembl
chr12:30763345..30764610hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231451
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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