A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025319



Internal ID21934662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98592687..98593394hg38UCSC Ensembl
chr15:99135916..99136623hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025319
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