A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590660



Internal ID20963731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66912601..66913717hg38UCSC Ensembl
chr15:67204939..67206055hg19UCSC Ensembl
Cytoband15q22.32
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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