A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092898



Internal ID22002131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45914212..45914212hg38UCSC Ensembl
chr17:43991578..43991578hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632636
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092898
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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