A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291786



Internal ID20501004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63547749..63547833hg38UCSC Ensembl
chr15:63839948..63840032hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733458
Supporting Variants
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291786
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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