A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915517



Internal ID22690735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14287331..14291390hg38UCSC Ensembl
chr9:14287330..14291389hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg384060
hg194060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446801
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915517
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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