A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835732



Internal ID22610667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194622881..194625730hg38UCSC Ensembl
chr3:194343610..194346459hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490418
Samples
Known GenesTMEM44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835732
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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