A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372122



Internal ID22597791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1513264..1514142hg38UCSC Ensembl
chr16:1563265..1564143hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946524
Supporting Variants
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372122
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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