A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225728



Internal ID22368771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109173888..109174770hg38UCSC Ensembl
chr13:109826236..109827118hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368598, nssv14368597, nssv14368596
SamplesHG00512, HG00513, HG00514
Known GenesMYO16
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225728
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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