A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489566



Internal ID22547485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120442796..120446083hg38UCSC Ensembl
chr3:120161643..120164930hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383288
hg193288
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834298
Supporting Variants
Samples
Known GenesFSTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489566
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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