A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101014



Internal ID20668054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53352916..53354429hg38UCSC Ensembl
chr3:53386943..53388456hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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