A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998878



Internal ID21908221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8758992..8759064hg38UCSC Ensembl
chr4:8760718..8760790hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998878
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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