A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482198



Internal ID259656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149055491..149059645hg38UCSC Ensembl
chr7:148752583..148756737hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384155
hg194155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482198
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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