A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196380



Internal ID20763420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107590601..107591800hg38UCSC Ensembl
chr11:107461327..107462526hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461774
Supporting Variants
Samples
Known GenesELMOD1, LOC643923
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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