A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001058



Internal ID21910401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:510469..510685hg38UCSC Ensembl
chr7:550106..550322hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563406
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001058
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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