A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387800



Internal ID22273761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65230438..65230904hg38UCSC Ensembl
chr15:65522776..65523242hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227923
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387800
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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