A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098833



Internal ID22008066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45941618..45941618hg38UCSC Ensembl
chr17:44018984..44018984hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635848
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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