A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733452



Internal ID20509382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9583749..9583816hg38UCSC Ensembl
chr11:9605296..9605363hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291405
Samples
Known GenesWEE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733452
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer