A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962518



Internal ID22737453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96602543..96602543hg38UCSC Ensembl
chr9:99364825..99364825hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430347
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962518
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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