A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1727n223



Internal ID22804695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126335742..126747623hg38UCSC Ensembl
chr12:126820288..127232169hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38411882
hg19411882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6495015, nsv6492805
Samples
Known GenesLINC00943, LINC00944, LOC100128554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1727n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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