A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284350



Internal ID20493568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52166815..52166815hg38UCSC Ensembl
chr7:52234511..52234511hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284350
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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