A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731653



Internal ID20507573
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 StatusM
Merged Variants
Supporting Variantsnssv16266774
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731653
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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