A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7475n223



Internal ID22810443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119233203..119237500hg38UCSC Ensembl
chr8:120245443..120249740hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg384298
hg194298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6431713, nsv6430880
Samples
Known GenesMAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7475n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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