A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7141n223



Internal ID22810109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142329053..142474236hg38UCSC Ensembl
chr7:142157709..142276197hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38145184
hg19118489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6423227, nsv6427029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7141n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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