A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020244



Internal ID21929587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:511263..511348hg38UCSC Ensembl
chr7:550900..550985hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576579
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020244
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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