A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180171



Internal ID20747211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102299022..102303476hg38UCSC Ensembl
chr11:102169753..102174207hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384455
hg194455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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