A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097209



Internal ID20664249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17145873..17148677hg38UCSC Ensembl
chr3:17187365..17190169hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382805
hg192805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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