A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485132



Internal ID262529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94818026..94827471hg38UCSC Ensembl
chr7:94447338..94456783hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg389446
hg199446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485132
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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