A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14367407



Internal ID22255944
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225681
Supporting Variants
SamplesNA19238
Known GenesNUPL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14367407
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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