A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368471



Internal ID22594140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120061467..120061947hg38UCSC Ensembl
chr11:119932176..119932656hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368471
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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