A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483536



Internal ID260972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133355208..133355802hg38UCSC Ensembl
chr7:133039962..133040556hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002713
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483536
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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