A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327462



Internal ID22276323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13064564..13064618hg38UCSC Ensembl
chr6:13064796..13064850hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209873
Supporting Variants
SamplesNA19239
Known GenesPHACTR1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327462
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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