A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864180



Internal ID22639115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27356026..27359062hg38UCSC Ensembl
chr11:27377573..27380609hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg383037
hg193037
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457724
Samples
Known GenesCCDC34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864180
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