A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023568



Internal ID21932911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40509282..40509564hg38UCSC Ensembl
chr17:38665534..38665816hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023568
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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