A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv491n206



Internal ID22755795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142560927..142796849hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38235923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6142123, nsv6142717, nsv6142526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv491n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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