A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210018



Internal ID20777058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54013857..54028658hg38UCSC Ensembl
chr3:54047884..54062685hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3814802
hg1914802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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