A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263842



Internal ID20473060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138329089..138329150hg38UCSC Ensembl
chr4:139250243..139250304hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747261
Supporting Variants
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263842
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