A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14289878



Internal ID22282536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8934744..8934846hg38UCSC Ensembl
chr18:8934742..8934844hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223910
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14289878
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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