A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592588



Internal ID20965659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48403150..48404151hg38UCSC Ensembl
chr10:49611193..49612194hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229365
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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