A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226880



Internal ID22369537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98049062..98049551hg38UCSC Ensembl
chr13:98701316..98701805hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14371763
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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