A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458028



Internal ID236061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22416314..22421525hg38UCSC Ensembl
chr7:22455933..22461144hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385212
hg195212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993890
Samples
Known GenesSTEAP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458028
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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