A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594017



Internal ID20967088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128624268..128626296hg38UCSC Ensembl
chr12:129108813..129110841hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg382029
hg192029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1733n223
Supporting Variantsnssv18225326
Samples
Known GenesTMEM132C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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