A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591649



Internal ID20964720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48421580..48422029hg38UCSC Ensembl
chr10:49629623..49630072hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223085
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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