A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486566



Internal ID263927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73809549..73809604hg38UCSC Ensembl
chr7:73223879..73223934hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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