A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089760



Internal ID21998993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64548405..64548405hg38UCSC Ensembl
chr17:62544523..62544523hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627947
Samples
Known GenesSMURF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089760
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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