A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522080



Internal ID21846439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13766797..13766797hg38UCSC Ensembl
chr1:14093292..14093292hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046053
Supporting Variants
Samples
Known GenesPRDM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522080
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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