A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082486



Internal ID21991719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111251913..111251913hg38UCSC Ensembl
chr9:114014193..114014193hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082486
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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