A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598638



Internal ID21790683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43508722..43509222hg38UCSC Ensembl
chr15:43800920..43801420hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031891
Supporting Variants
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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