A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899466



Internal ID22674596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151793535..151793602hg38UCSC Ensembl
chr5:151173096..151173163hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409751
Samples
Known GenesG3BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899466
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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