A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573768



Internal ID20946839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87565847..87581420hg38UCSC Ensembl
chr9:90180762..90196335hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3815574
hg1915574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281330
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573768
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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