A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368521



Internal ID22136924
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228328
Supporting Variants
SamplesHG00513
Known GenesLECT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368521
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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