A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593959



Internal ID20967030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12118112..12119468hg38UCSC Ensembl
chr10:12160111..12161467hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225242
Samples
Known GenesDHTKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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