A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099691



Internal ID22008924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16665896..16665896hg38UCSC Ensembl
chr17:16569210..16569210hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099691
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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