A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278401



Internal ID20487619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64799172..64799251hg38UCSC Ensembl
chr15:65091371..65091450hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278401
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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