A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063444



Internal ID21972677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80825074..80825074hg38UCSC Ensembl
chr7:80454390..80454390hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565960
Samples
Known GenesSEMA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063444
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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