A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228328



Internal ID22370549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707298..52707410hg38UCSC Ensembl
chr13:53281433..53281545hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368521, nssv14368522
SamplesHG00513, HG00514
Known GenesLECT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228328
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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