A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028093



Internal ID21937436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45205074..45209815hg38UCSC Ensembl
chr17:43282441..43287182hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384742
hg194742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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