A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579867



Internal ID20952938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110055214..110056072hg38UCSC Ensembl
chr12:110493019..110493877hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1687n223
Supporting Variantsnssv18230997
Samples
Known GenesC12orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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