A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451128



Internal ID22509000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3383791..3384990hg38UCSC Ensembl
chr11:3405021..3406220hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852725
Supporting Variants
Samples
Known GenesLOC650368
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451128
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