A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027836



Internal ID21937179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93185244..93222399hg38UCSC Ensembl
chr15:93728473..93765628hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3837156
hg1937156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027836
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