A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv810n223



Internal ID22803778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73592601..73761100hg38UCSC Ensembl
chr10:75352359..75520858hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38168500
hg19168500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6451819, nsv6444761, nsv6441859
Samples
Known GenesAGAP5, BMS1P4, GLUD1P3, MYOZ1, SEC24C, SYNPO2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv810n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer