A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459076



Internal ID22516958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83256814..83268134hg38UCSC Ensembl
chr11:82967856..82979176hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811321
hg1911321
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847598
Supporting Variants
Samples
Known GenesCCDC90B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459076
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