A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387367



Internal ID22182550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26939842..26957961hg38UCSC Ensembl
chr17:25266868..25284987hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3818120
hg1918120
Variant TypeCNV duplication
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229194
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387367
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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