A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226640



Internal ID22369372
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367501, nssv14367500
SamplesHG00731, HG00732
Known GenesPAN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226640
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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