A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647249



Internal ID21839296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42349641..42349641hg38UCSC Ensembl
chr21:43769750..43769750hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103385
Supporting Variants
Samples
Known GenesTFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647249
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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