A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7771n223



Internal ID22810739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63694501..63862700hg38UCSC Ensembl
chr9:68290235..68458434hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38168200
hg19168200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6448076, nsv6446660
Samples
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7771n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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