A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576981



Internal ID20950052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69406875..69407188hg38UCSC Ensembl
chr15:69699214..69699527hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239636
Samples
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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