A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380236



Internal ID22209136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89765301..89768900hg38UCSC Ensembl
chr15:90308532..90312131hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216287
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380236
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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