A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7156n223



Internal ID22810124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143165801..143203100hg38UCSC Ensembl
chr7:142862894..142900193hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3837300
hg1937300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6423936, nsv6418752
Samples
Known GenesTAS2R39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7156n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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