A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102203



Internal ID20669243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50140009..50140375hg38UCSC Ensembl
chr3:50177442..50177808hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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