A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211196



Internal ID20778236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3840409..3856108hg38UCSC Ensembl
chr3:3882093..3897792hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3815700
hg1915700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363820
Supporting Variants
Samples
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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