A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301376



Internal ID22220156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11547399..11554787hg38UCSC Ensembl
chrUn_gl000232:62..7450hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387389
hg197389
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227346
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301376
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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