A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379964



Internal ID22173454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69463701..69464370hg38UCSC Ensembl
chr15:69756040..69756709hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215814
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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