A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592274



Internal ID20965345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54261047..54261586hg38UCSC Ensembl
chr12:54654831..54655370hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1545n223
Supporting Variantsnssv18217140
Samples
Known GenesCBX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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