A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1947n209



Internal ID22828022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155225916..155227287hg38UCSC Ensembl
chr7:155017626..155018997hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5925601, nsv5923887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1947n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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