A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305909



Internal ID22204194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58162465..58163719hg38UCSC Ensembl
chr3:58148192..58149446hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204280
Supporting Variants
SamplesHG00732
Known GenesFLNB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305909
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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