A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834274



Internal ID22609209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111071352..111072649hg38UCSC Ensembl
chr3:110790199..110791496hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483751, nssv17483750
Samples
Known GenesPVRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834274
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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