A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278154



Internal ID20487372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78090053..78098120hg38UCSC Ensembl
chr10:79849810..79857877hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg388068
hg198068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278154
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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