A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283777



Internal ID20492995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101163115..101163115hg38UCSC Ensembl
chr8:102175343..102175343hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283777
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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