A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384895



Internal ID22268330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13501228..13501334hg38UCSC Ensembl
chr17:13404545..13404651hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213433
Supporting Variants
SamplesNA19238
Known GenesHS3ST3A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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