A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6654n223



Internal ID22809622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39599101..39633700hg38UCSC Ensembl
chr7:39638700..39673299hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3834600
hg1934600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6617283, nsv6603641
Samples
Known GenesRALA, YAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6654n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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