A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568610



Internal ID21760653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5507833..5507833hg38UCSC Ensembl
chr7:5547464..5547464hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064262
Supporting Variants
Samples
Known GenesFBXL18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568610
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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