A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380547



Internal ID22285670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95211312..95211369hg38UCSC Ensembl
chr15:95754541..95754598hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527102
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380547
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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