A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834689



Internal ID22609624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142131184..142133683hg38UCSC Ensembl
chr3:141850026..141852525hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485200
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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