A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998113



Internal ID21907456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76775932..76776088hg38UCSC Ensembl
chr4:77697085..77697241hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557321
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998113
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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