A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915568



Internal ID22690786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111050494..111051133hg38UCSC Ensembl
chr9:113812774..113813413hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915568
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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