A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579246



Internal ID20952317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59680167..59703083hg38UCSC Ensembl
chr10:61439925..61462841hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3822917
hg1922917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222807
Samples
Known GenesSLC16A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579246
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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