A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081396



Internal ID21490305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38448801..38448801hg38UCSC Ensembl
chr17:36605045..36605045hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644923
Supporting Variants
SamplesNA19238
Known GenesARHGAP23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081396
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer