A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189309



Internal ID20756349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95475801..95486000hg38UCSC Ensembl
chr11:95208965..95219164hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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