A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458598



Internal ID22516481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222259..35233743hg38UCSC Ensembl
chr11:35243806..35255290hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811485
hg1911485
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848017
Supporting Variants
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458598
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