A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233855



Internal ID20800895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113187665..113187861hg38UCSC Ensembl
chr12:113625470..113625666hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593936
Supporting Variants
Samples
Known GenesC12orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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