A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281292



Internal ID20490510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56635282..56635282hg38UCSC Ensembl
chr1:57100955..57100955hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381953
hg191953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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