A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099587



Internal ID20666627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18720001..18827100hg38UCSC Ensembl
chr3:18761493..18868592hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38107100
hg19107100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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