A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359956



Internal ID22585625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222308..35237977hg38UCSC Ensembl
chr11:35243855..35259524hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815670
hg1915670
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918306
Supporting Variants
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359956
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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