A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14309308



Internal ID22274221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120442802..120446104hg38UCSC Ensembl
chr3:120161649..120164951hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383303
hg193303
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205137
Supporting Variants
SamplesNA19239
Known GenesFSTL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14309308
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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