A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579265



Internal ID20952336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114181812..114182928hg38UCSC Ensembl
chr10:115941571..115942687hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229520
Samples
Known GenesTDRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579265
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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