A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086716



Internal ID21995949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56621862..56621862hg38UCSC Ensembl
chr17:54699223..54699223hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086716
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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