A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580008



Internal ID20953079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110360180..110361216hg38UCSC Ensembl
chr12:110797985..110799021hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381037
hg191037
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n223
Supporting Variantsnssv18231892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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