A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590002



Internal ID20963073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104338465..104339076hg38UCSC Ensembl
chr12:104732243..104732854hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226363
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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