A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278898



Internal ID20488116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47084517..47084593hg38UCSC Ensembl
chr2:47311656..47311732hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278898
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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