A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994630



Internal ID21903973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100195563..100195690hg38UCSC Ensembl
chr4:101116720..101116847hg19UCSC 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 Variantsnssv17553760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994630
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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