A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155373



Internal ID22085878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10268167..10295614hg38UCSC Ensembl
Outerchr17:10266808..10298798hg38UCSC Ensembl
Innerchr17:10171484..10198931hg19UCSC Ensembl
Outerchr17:10170125..10202115hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3831991
hg1931991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv126n97
Supporting Variantsnssv4010082, nssv4010081
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155373
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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