A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889235



Internal ID22664250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112005865..112005921hg38UCSC Ensembl
chr3:111724712..111724768hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399273
Samples
Known GenesTAGLN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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