A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7908n223



Internal ID22810876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110159107..110309700hg38UCSC Ensembl
chr9:112921387..113071980hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38150594
hg19150594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6437552, nsv6441527
Samples
Known GenesAKAP2, C9orf152, PALM2-AKAP2, TXN, TXNDC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7908n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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