A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747667



Internal ID20523687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106824721..106824883hg38UCSC Ensembl
chr7:106465167..106465329hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747667
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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