A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738144



Internal ID20514111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119449474..119449529hg38UCSC Ensembl
chr3:119168321..119168376hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276955
Samples
Known GenesTMEM39A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738144
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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