A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6590n223



Internal ID22809558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13180912..13272590hg38UCSC Ensembl
chr7:13220537..13312215hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3891679
hg1991679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6608209, nsv6619489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6590n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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