A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995533



Internal ID21904876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791368..15791447hg38UCSC Ensembl
chr4:15792991..15793070hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555767
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995533
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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