A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013914



Internal ID21923257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111050495..111051137hg38UCSC Ensembl
chr9:113812775..113813417hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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