A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14287283



Internal ID22255838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19665089..19665431hg38UCSC Ensembl
chr19:19775898..19776240hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229976
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14287283
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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