A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595196



Internal ID20968267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52051858..52053102hg38UCSC Ensembl
chr15:52344055..52345299hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240362
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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