A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589936



Internal ID20963007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68831431..68831879hg38UCSC Ensembl
chr15:69123770..69124218hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239627
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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