A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155483



Internal ID22085988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53753044..53788567hg38UCSC Ensembl
Outerchr17:53750525..53790280hg38UCSC Ensembl
Innerchr17:51830405..51865928hg19UCSC Ensembl
Outerchr17:51827886..51867641hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3839756
hg1939756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011862
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155483
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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