A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593019



Internal ID20966090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113755463..113756241hg38UCSC Ensembl
chr10:115515222..115516000hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235182
Samples
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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