A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270428



Internal ID20479646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59769203..59769203hg38UCSC Ensembl
chr15:60061402..60061402hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270428
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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