A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019557



Internal ID21928900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114938126..114940361hg38UCSC Ensembl
chr9:117700406..117702641hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382236
hg192236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019557
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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