A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967009



Internal ID22741944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107305944..107305944hg38UCSC Ensembl
chr9:110068225..110068225hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432109
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967009
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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