A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447159



Internal ID21104712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110853167..110873012hg38UCSC Ensembl
chr9:113615447..113635292hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3819846
hg1919846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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