A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285707



Internal ID20494925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20981448..20981575hg38UCSC Ensembl
chr1:21307941..21308068hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748531
Supporting Variants
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285707
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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