A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071541



Internal ID21980774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:510763..510763hg38UCSC Ensembl
chr7:550400..550400hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573432
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071541
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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