A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190139



Internal ID21328987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120413799..120413799hg38UCSC Ensembl
chr3:120132646..120132646hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935766
Supporting Variants
SamplesHG002
Known GenesFSTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190139
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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