A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020343



Internal ID21929686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42926279..42926351hg38UCSC Ensembl
chr7:42965878..42965950hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564492
Samples
Known GenesPSMA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020343
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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