A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365489



Internal ID22591158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30866920..30936393hg38UCSC Ensembl
chr11:30888467..30957940hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3869474
hg1969474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923173
Supporting Variants
Samples
Known GenesDCDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365489
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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