A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219008



Internal ID22364165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27184672..27184823hg38UCSC Ensembl
chr13:27758809..27758960hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367457, nssv14367456, nssv14367458
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219008
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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