A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368643



Internal ID22307987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109665951..109666011hg38UCSC Ensembl
chr13:110318298..110318358hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219886
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368643
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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