A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574967



Internal ID21523390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35640580..35640688hg38UCSC Ensembl
chr1:36106181..36106289hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065160
SamplesHG00513
Known GenesPSMB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574967
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