A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100962



Internal ID20668002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52287555..52288105hg38UCSC Ensembl
chr3:52321571..52322121hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356960
Supporting Variants
Samples
Known GenesGLYCTK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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