A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081153



Internal ID21990386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62888119..62888119hg38UCSC Ensembl
chr17:60965480..60965480hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624132
Samples
Known GenesMIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081153
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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