A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451226



Internal ID22509098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44091917..44093816hg38UCSC Ensembl
chr11:44113467..44115366hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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