A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035831



Internal ID21945174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42351150..42373376hg38UCSC Ensembl
chr17:40503168..40525394hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3822227
hg1922227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623438
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035831
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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