A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174477



Internal ID20741517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102554376..102609908hg38UCSC Ensembl
chr9:105316658..105372190hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3855533
hg1955533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451619
Supporting Variants
Samples
Known GenesLINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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