A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357809



Internal ID22583478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92753798..92753798hg38UCSC Ensembl
chr11:92486964..92486964hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976294
Supporting Variants
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357809
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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