A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020003



Internal ID21929346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125279599..125607544hg38UCSC Ensembl
chr7:124919653..125247598hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38327946
hg19327946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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