A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587896



Internal ID20960967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118202782..118203721hg38UCSC Ensembl
chr12:118640587..118641526hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1704n223
Supporting Variantsnssv18233411
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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