A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997055



Internal ID21906398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3790114..3798638hg38UCSC Ensembl
chr4:3791841..3800365hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388525
hg198525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997055
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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