A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360281



Internal ID22585950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77646734..77646734hg38UCSC Ensembl
chr11:77357779..77357779hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360281
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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