A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv726n223



Internal ID22803694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47642201..47713200hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3871000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6441728, nsv6436626, nsv6444269, nsv6442950, nsv6439581, nsv6442426, nsv6449580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv726n223
Frequency
Sample Size19652
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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