A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602589



Internal ID21551248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79709602..79710164hg38UCSC Ensembl
chr17:77683410..77683972hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079701
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602589
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