A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835138



Internal ID22610073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177190192..177193146hg38UCSC Ensembl
chr3:176907980..176910934hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382955
hg192955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489707
Samples
Known GenesTBL1XR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835138
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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