A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962473



Internal ID22737408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149322905..149322905hg38UCSC Ensembl
chr3:149040692..149040692hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417588
Samples
Known GenesTM4SF18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962473
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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