A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259337



Internal ID20468555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28520960..28520960hg38UCSC Ensembl
chr4:28522582..28522582hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259337
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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