A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294249



Internal ID20503467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17085167..17085249hg38UCSC Ensembl
chr21:18457485..18457567hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294249
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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