A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280717



Internal ID20489935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32300691..32300691hg38UCSC Ensembl
chr21:33673002..33673002hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764272
Supporting Variants
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280717
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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