A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589567



Internal ID20962638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44521938..44523048hg38UCSC Ensembl
chr15:44814136..44815246hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240253
Samples
Known GenesCTDSPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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