A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209276



Internal ID20776316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45506627..45604642hg38UCSC Ensembl
chr3:45548119..45646134hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3898016
hg1998016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365579
Supporting Variants
Samples
Known GenesLARS2, LARS2-AS1, LIMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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