A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032254



Internal ID21941597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99927890..99927963hg38UCSC Ensembl
chr14:100394227..100394300hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607573
Samples
Known GenesEML1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032254
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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