A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267035



Internal ID20476253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44651857..44651857hg38UCSC Ensembl
chr17:42729225..42729225hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267035
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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