A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099774



Internal ID20666814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179476706..179481698hg38UCSC Ensembl
chr3:179194494..179199486hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384993
hg194993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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