A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994768



Internal ID21904111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100996357..100996433hg38UCSC Ensembl
chr4:101917514..101917590hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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