A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099247



Internal ID20666287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30235286..30235873hg38UCSC Ensembl
chr3:30276777..30277364hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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