A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373777



Internal ID22599446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26646978..26653612hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373777
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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