A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178923



Internal ID20745963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86622..258649hg38UCSC Ensembl
chr9:86622..258649hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38172028
hg19172028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426659
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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