A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099413



Internal ID21493046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59500450..59500499hg38UCSC Ensembl
chr17:57577811..57577860hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598326
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099413
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