A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101005



Internal ID20668045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53237744..53242384hg38UCSC Ensembl
chr3:53271760..53276400hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg384641
hg194641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357735
Supporting Variants
Samples
Known GenesTKT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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