A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485151



Internal ID22543062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138389428..138399207hg38UCSC Ensembl
chr3:138108270..138118049hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg389780
hg199780
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834939
Supporting Variants
Samples
Known GenesMRAS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485151
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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