A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484795



Internal ID262200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98734022..98738071hg38UCSC Ensembl
chr7:98363334..98367383hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484795
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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