A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025368



Internal ID21934711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58750756..58750892hg38UCSC Ensembl
chr15:59042955..59043091hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025368
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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