A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005908



Internal ID21915251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8092772..8102597hg38UCSC Ensembl
chr6:8093005..8102830hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg389826
hg199826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558307
Samples
Known GenesEEF1E1, EEF1E1-BLOC1S5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005908
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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