A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14367501



Internal ID22204534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28141114..28141484hg38UCSC Ensembl
chr13:28715251..28715621hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226640
Supporting Variants
SamplesHG00732
Known GenesPAN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14367501
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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