A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293741



Internal ID20502959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87616787..87616787hg38UCSC Ensembl
chr8:88629015..88629015hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293741
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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