A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026092



Internal ID21935435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10267903..10297720hg38UCSC Ensembl
chr17:10171220..10201037hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3829818
hg1929818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026092
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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