A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281710



Internal ID20490928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209990536..209990536hg38UCSC Ensembl
chr1:210163881..210163881hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751886
Supporting Variants
Samples
Known GenesSYT14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281710
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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