A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746579



Internal ID20522593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89474816..89474869hg38UCSC Ensembl
chr15:90018047..90018100hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273920
Samples
Known GenesRHCG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746579
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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