A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405537



Internal ID22463407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15514114..15514188hg38UCSC Ensembl
chr21:16886433..16886507hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405537
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009


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