A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733154



Internal ID20509081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22029125..22029278hg38UCSC Ensembl
chr7:22068743..22068896hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733154
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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