A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099274



Internal ID22008507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66209565..66209565hg38UCSC Ensembl
chr17:64205683..64205683hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382389
hg192389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099274
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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