A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182416



Internal ID20749456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95931592..95940930hg38UCSC Ensembl
chr11:95664756..95674094hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389339
hg199339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182416
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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