A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668828



Internal ID21617133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1174002..1174208hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169550
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668828
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