A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591364



Internal ID20964435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68217610..68218481hg38UCSC Ensembl
chr15:68509948..68510819hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239619
Samples
Known GenesCLN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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