A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7693n223



Internal ID22810661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34197950..34444322hg38UCSC Ensembl
chr9:34197948..34444320hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38246373
hg19246373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6440375, nsv6449868
Samples
Known GenesC9orf24, FAM219A, KIAA1161, KIF24, NUDT2, UBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7693n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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