A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289144



Internal ID20498362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42848380..42848609hg38UCSC Ensembl
chr21:44268490..44268719hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735906
Supporting Variants
Samples
Known GenesWDR4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289144
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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