A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7417n223



Internal ID22810385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89895701..89908200hg38UCSC Ensembl
chr8:90907929..90920428hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6429368, nsv6421926
Samples
Known GenesOSGIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7417n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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