A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617751



Internal ID21809798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14184049..14184049hg38UCSC Ensembl
chr17:14087366..14087366hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091742
Supporting Variants
Samples
Known GenesCOX10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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