A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955407



Internal ID22730609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141977089..141977089hg38UCSC Ensembl
chr3:141695931..141695931hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390633
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955407
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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