A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084783



Internal ID21994016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64026604..64026604hg38UCSC Ensembl
chr17:62103964..62103964hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084783
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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