A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282247



Internal ID20491465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56585575..56585721hg38UCSC Ensembl
chr15:56877773..56877919hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282247
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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