A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732226



Internal ID20508149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39545533..39547088hg38UCSC Ensembl
chr15:39837734..39839289hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381556
hg191556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732226
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer