A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591628



Internal ID21540205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91389473..91389643hg38UCSC Ensembl
chr10:93149230..93149400hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072262
SamplesHG02818
Known GenesLOC100188947
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591628
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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