A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591039



Internal ID21539611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43975862..43975965hg38UCSC Ensembl
chr17:42053230..42053333hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086727
SamplesHG00731
Known GenesPYY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591039
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