A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7807n223



Internal ID22810775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65703501..65745700hg38UCSC Ensembl
chr9:42684421..42726620hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3842200
hg1942200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6444434, nsv6453182, nsv6444650, nsv6449039
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7807n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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