A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265313



Internal ID20474531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39705759..39705917hg38UCSC Ensembl
chr4:39707379..39707537hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744435
Supporting Variants
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265313
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