A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269593



Internal ID20478811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41828914..41828914hg38UCSC Ensembl
chr21:43249270..43249270hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763230
Supporting Variants
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269593
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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