A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7819n223



Internal ID22810787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71101404..71879773hg38UCSC Ensembl
chr9:73716320..74494689hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38778370
hg19778370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6446224, nsv6443841
Samples
Known GenesABHD17B, TMEM2, TRPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7819n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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