A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287834



Internal ID20497052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68860132..68860309hg38UCSC Ensembl
chr15:69152471..69152648hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731101
Supporting Variants
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287834
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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