A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590813



Internal ID20963884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64491459..64492558hg38UCSC Ensembl
chr12:64885239..64886338hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230165
Samples
Known GenesTBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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