A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072010



Internal ID21457720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94334791..94334791hg38UCSC Ensembl
chr10:96094548..96094548hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631030
Supporting Variants
SamplesHG02587
Known GenesNOC3L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072010
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