A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068341



Internal ID21461554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11354385..11354385hg38UCSC Ensembl
chr10:11396384..11396384hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643450
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068341
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