A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104947



Internal ID20671987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9873569..9877177hg38UCSC Ensembl
chr3:9915253..9918861hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383609
hg193609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373575
Supporting Variants
Samples
Known GenesCIDEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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