A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266774



Internal ID20475992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43451967..43452159hg38UCSC Ensembl
chr15:43744165..43744357hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731653
Supporting Variants
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266774
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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