A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283368



Internal ID20492586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101096435..101096435hg38UCSC Ensembl
chr1:101561991..101561991hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283368
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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