A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629260



Internal ID21821307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57915232..57915232hg38UCSC Ensembl
chr17:55992593..55992593hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092250
Supporting Variants
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629260
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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