A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834189



Internal ID22609124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105447642..105448841hg38UCSC Ensembl
chr3:105166486..105167685hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483673
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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