A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492476



Internal ID22550403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45501764..45510560hg38UCSC Ensembl
chr3:45543256..45552052hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388797
hg198797
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836561
Supporting Variants
Samples
Known GenesLARS2, LARS2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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