A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070923



Internal ID21980156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35835151..35835151hg38UCSC Ensembl
chr7:35874761..35874761hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564511
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070923
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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