A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995052



Internal ID21904395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100195488..100195615hg38UCSC Ensembl
chr4:101116645..101116772hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995052
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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