A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384191



Internal ID22210048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81062969..81067820hg38UCSC Ensembl
chr15:81355310..81360161hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227213
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384191
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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