A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593808



Internal ID20966879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58921933..58922486hg38UCSC Ensembl
chr15:59214132..59214685hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241171
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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