A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370289



Internal ID21027842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168590573..168630655hg38UCSC Ensembl
chr3:168308361..168348443hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3840083
hg1940083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097367
Samples
Known GenesEGFEM1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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