A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994767



Internal ID21904110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1007665..1007816hg38UCSC Ensembl
chr4:1001453..1001604hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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