A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1229n223



Internal ID22804197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74307301..74335900hg38UCSC Ensembl
chr11:74018346..74046945hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3828600
hg1928600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6463437, nsv6470412
Samples
Known GenesP4HA3, PGM2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1229n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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