A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584739



Internal ID20957810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118693529..118695083hg38UCSC Ensembl
chr12:119131334..119132888hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381555
hg191555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1706n223
Supporting Variantsnssv18230114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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