A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025109



Internal ID21934452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114014065..114050663hg38UCSC Ensembl
chr11:113884787..113921385hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3836599
hg1936599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025109
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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