A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231766



Internal ID20798806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128112060..128113241hg38UCSC Ensembl
chr12:128596605..128597786hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575810
Supporting Variants
Samples
Known GenesLOC100996679
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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