A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069454



Internal ID21978687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23507864..23507864hg38UCSC Ensembl
chr7:23547483..23547483hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558062
Samples
Known GenesTRA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069454
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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