A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1908n209



Internal ID22827983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76319784..76320669hg38UCSC Ensembl
chr7:75949101..75949986hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5924862, nsv5918141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1908n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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