A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451713



Internal ID22509585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99424779..99425878hg38UCSC Ensembl
chr11:99295510..99296609hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860132
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451713
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