A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995126



Internal ID21904469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1335591..1335670hg38UCSC Ensembl
chr4:1329379..1329458hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548697
Samples
Known GenesMAEA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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