A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483751



Internal ID22541658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111071352..111072649hg38UCSC Ensembl
chr3:110790199..110791496hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834274
Supporting Variants
Samples
Known GenesPVRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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