A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586968



Internal ID20960039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11578555..11579011hg38UCSC Ensembl
chr12:11731489..11731945hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1421n223
Supporting Variantsnssv18230167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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