A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291083



Internal ID20500301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41383286..41383465hg38UCSC Ensembl
chr15:41675484..41675663hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291083
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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