A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093282



Internal ID22002515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48810823..48810823hg38UCSC Ensembl
chr17:46888185..46888185hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628054
Samples
Known GenesTTLL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093282
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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