A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293831



Internal ID20503049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69611997..69611997hg38UCSC Ensembl
chr17:67608138..67608138hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293831
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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