A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7673n223



Internal ID22810641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28600671..28814968hg38UCSC Ensembl
chr9:28600669..28814966hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38214298
hg19214298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6428337, nsv6425452
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7673n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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