A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069194



Internal ID21978427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129147157..129147157hg38UCSC Ensembl
chr7:128786998..128786998hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557850
Samples
Known GenesTSPAN33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069194
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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