A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744435



Internal ID20520434
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 StatusM
Merged Variants
Supporting Variantsnssv16265313
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744435
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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