A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225681



Internal ID22368742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25309792..25309851hg38UCSC Ensembl
chr13:25883930..25883989hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367407
SamplesNA19238
Known GenesNUPL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225681
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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