A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474245



Internal ID251908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143419751..143420566hg38UCSC Ensembl
chr7:143116844..143117659hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003849
Samples
Known GenesEPHA1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474245
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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