A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010080



Internal ID22071711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10268167..10295268hg38UCSC Ensembl
Outerchr17:10266808..10295512hg38UCSC Ensembl
Innerchr17:10171484..10198585hg19UCSC Ensembl
Outerchr17:10170125..10198829hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3828705
hg1928705
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155372
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010080
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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