A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564511



Internal ID21888866
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 StatusS
Merged Variantsnsv6070923
Supporting Variants
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564511
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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