A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591694



Internal ID20964765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101800795..101801386hg38UCSC Ensembl
chr10:103560552..103561143hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225039
Samples
Known GenesMGEA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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