A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995281



Internal ID21904624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152777205..152777267hg38UCSC Ensembl
chr4:153698357..153698419hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545953
Samples
Known GenesTIGD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995281
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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