A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281562



Internal ID20848602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96578892..96579474hg38UCSC Ensembl
chr9:99341174..99341756hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566536
Supporting Variants
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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