A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565374



Internal ID21513686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62759809..62759868hg38UCSC Ensembl
chr1:63225480..63225539hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066191
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565374
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