A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288146



Internal ID20497364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35239043..35243829hg38UCSC Ensembl
chr15:35531244..35536030hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384787
hg194787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288146
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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