A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7812n223



Internal ID22810780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146401..66152400hg38UCSC Ensembl
chr9:42368869..42374865hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386000
hg195997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6447205, nsv6453557, nsv6452035
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7812n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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