A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7490n223



Internal ID22810458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128241201..128278300hg38UCSC Ensembl
chr8:129253447..129290546hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3837100
hg1937100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6431392, nsv6431471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7490n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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