A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7767n223



Internal ID22810735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63542401..63600300hg38UCSC Ensembl
chr9:68138135..68196034hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3857900
hg1957900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6442862, nsv6439655, nsv6439097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7767n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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