A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355915



Internal ID22581584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65673481..65673988hg38UCSC Ensembl
chr11:65440952..65441459hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355915
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005


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