A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029945



Internal ID21939288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43451962..43452154hg38UCSC Ensembl
chr15:43744160..43744352hg19UCSC 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 Variantsnssv17610785
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029945
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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