A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183540



Internal ID20750580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42223..258291hg38UCSC Ensembl
chr9:42223..258291hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38216069
hg19216069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435466
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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