A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502329



Internal ID279199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43508723..43509222hg38UCSC Ensembl
chr15:43800921..43801420hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702014
Samples
Known GenesRNU6-28P, TP53BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502329
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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