A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083902



Internal ID21993135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74302033..74302033hg38UCSC Ensembl
chr17:72298172..72298172hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636315
Samples
Known GenesDNAI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083902
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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