A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073448



Internal ID21443234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124443032..124443032hg38UCSC Ensembl
chr11:124312928..124312928hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658207
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073448
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