A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085485



Internal ID21445825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16689347..16689919hg38UCSC Ensembl
chr17:16592661..16593233hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604367
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085485
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