A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161453



Internal ID21493516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26104593..26104648hg38UCSC Ensembl
chr9:26104591..26104646hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601779
Supporting Variants
SamplesNA19238
Known GenesLOC100506422
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161453
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