A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997139



Internal ID21906482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23615397..23620379hg38UCSC Ensembl
chr4:23617020..23622002hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384983
hg194983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997139
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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