A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296662



Internal ID20505880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115075991..115075991hg38UCSC Ensembl
chr8:116088220..116088220hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296662
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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