A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070193



Internal ID21464651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38063979..38063979hg38UCSC Ensembl
chr10:38352907..38352907hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381982
hg191982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635269
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070193
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