A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060714



Internal ID21969947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16673..16673hg38UCSC Ensembl
chr7:16673..16673hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060714
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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