A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503894



Internal ID20877152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88627744..88628225hg38UCSC Ensembl
chr14:89094088..89094569hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021605
Samples
Known GenesEML5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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