A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025384



Internal ID21934727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88789470..88789581hg38UCSC Ensembl
chr14:89255814..89255925hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603383
Samples
Known GenesEML5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025384
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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